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    {
        "title": "Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). An intermediate clinical phenotype caused by substitution of valine for glycine at position 137 of arylsulfatase B.",
        "journal": "The Journal of biological chemistry",
        "date": "1991",
        "authors": "Wicker G, Prill V, Brooks D, Gibson G, Hopwood J, von Figura K, Peters C",
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            "id": "1718978",
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            }
        ],
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                ],
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            }
        ],
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            {
                "evidence": [
                    {
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                        "database": "dbSNP",
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                    {
                        "id": "rs118203938",
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                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs118203938"
                    },
                    {
                        "id": "rs118203938",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs118203938#frequency_tab"
                    },
                    {
                        "id": "rs118203938",
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                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs118203938"
                    },
                    {
                        "id": "1718978",
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                        "url": "https://pubmed.ncbi.nlm.nih.gov/1718978"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 137,
                "end_pos": 137,
                "sequence_org": "G",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, arylsulfatase.",
                "chr_id": "5",
                "chr_pos": "78969095",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G137",
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                    {
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                        "recommended_name": {
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                            "name": "mucopolysaccharidosis VI",
                            "description": "A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme N-acetylgalactosamine 4-sulfatase."
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                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
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                            },
                            {
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                            },
                            {
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                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
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                                "description": ""
                            },
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "deficiency of N-acetylgalactosamine-4-sulfatase",
                                "description": ""
                            },
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                                "resource": "MONDO",
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                                "description": "Mucopolysaccharidosis type 6 (MPS 6) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate."
                            },
                            {
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                                "resource": "MONDO",
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                            },
                            {
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                            },
                            {
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                            },
                            {
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
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                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "Maroteaux Lamy Syndrome",
                                "description": ""
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                            {
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                            {
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                            },
                            {
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                            },
                            {
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                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
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                            },
                            {
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                                "resource": "MONDO",
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                                "name": "Mucopoly-saccharidosis type VI",
                                "description": ""
                            },
                            {
                                "id": "MIM:253200",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/253200",
                                "name": "Mucopolysaccharidosis 6",
                                "description": "Mucopolysaccharidosis 6"
                            }
                        ],
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                                "database": "AGR",
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                            },
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                                "id": "12800",
                                "database": "AGR",
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                        ]
                    }
                ],
                "keywords": [
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                    "disease"
                ],
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        "title": "Segregation analysis in a family at risk for the Maroteaux-Lamy syndrome conclusively reveals c.1151G>A (p.S384N) as to be a polymorphism.",
        "journal": "European journal of human genetics : EJHG",
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                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Identification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patients.",
        "journal": "American journal of human genetics",
        "date": "1996",
        "authors": "Litjens T, Brooks DA, Peters C, Gibson GJ, Hopwood JJ",
        "reference": {
            "type": "PubMed",
            "id": "8651289",
            "url": "https://pubmed.ncbi.nlm.nih.gov/8651289"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P15848-1",
                "protein_name": "Arylsulfatase B",
                "gene_name": "ARSB",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P15848",
                        "url": "https://www.uniprot.org/uniprotkb/P15848"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs118203943",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs118203943"
                    },
                    {
                        "id": "rs118203943",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs118203943"
                    },
                    {
                        "id": "rs118203943",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs118203943#frequency_tab"
                    },
                    {
                        "id": "rs118203943",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs118203943"
                    },
                    {
                        "id": "8651289",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/8651289"
                    },
                    {
                        "id": "rs118203943",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs118203943"
                    }
                ],
                "glycoeffect": [
                    "n-glyco-sequon-gain",
                    "o-glyco-site-loss"
                ],
                "start_pos": 210,
                "end_pos": 210,
                "sequence_org": "Y",
                "sequence_mut": "C",
                "comment": "Somatic mutation passed 2 filters: n-glyco-sequon-gain (NMY->NMC); glycogene of type=glycogene, arylsulfatase.",
                "chr_id": "5",
                "chr_pos": "78964477",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y210",
                "keywords": [
                    "ebi",
                    "somatic",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:10581",
                        "recommended_name": {
                            "id": "DOID:10581",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10581",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10581",
                                "name": "MLD",
                                "description": ""
                            },
                            {
                                "id": "DOID:10581",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10581",
                                "name": "Scholz cerebral sclerosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:10581",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10581",
                                "name": "arylsulfatase A deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:10581",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10581",
                                "name": "deficiency of cerebroside-sulfatase",
                                "description": ""
                            },
                            {
                                "id": "DOID:10581",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10581",
                                "name": "sulfatide lipoidosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009590",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009590",
                                "name": "metachromatic leukodystrophy due to saposin B deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009590",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009590",
                                "name": "metachromatic leukodystrophy due to sap-B deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009590",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009590",
                                "name": "metachromatic leukodystrophy due to saposin b deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "metachromatic leukodystrophy, juvenile form",
                                "description": "Metachromatic leukodystrophy is an inherited condition characterized by the accumulation of fats called sulfatides in cells, especially cells of the nervous system. This accumulation results in progressive destruction of white matter of the brain, which consists of nerve fibers covered by myelin.Affected individuals experience progressive deterioration of intellectual functions and motor skills, such as the ability to walk. They also develop loss of sensation in the extremities, incontinence, seizures, paralysis, inability to speak, blindness, and hearing loss. Eventually they lose awareness of their surroundings and become unresponsive. This condition is inherited in an autosomal recessive pattern and is caused by mutations in the ARSA and PSAP genes."
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "MLD, juvenile form",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "arylsulfatase A deficiency, juvenile form",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "metachromatic leukodystrophy, juvenile form",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "ARSA deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "MLD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "arylsulfatase A deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "cerebral sclerosis diffuse metachromatic form",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "cerebroside sulfatase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "leukodystrophy metachromatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "metachromatic leukoencephalopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009591",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009591",
                                "name": "sulfatide lipidosis",
                                "description": ""
                            },
                            {
                                "id": "MIM:249900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/249900",
                                "name": "Metachromatic leukodystrophy due to saposin B deficiency",
                                "description": "Metachromatic leukodystrophy due to saposin B deficiency"
                            },
                            {
                                "id": "MIM:250100",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/250100",
                                "name": "Metachromatic leukodystrophy",
                                "description": "Metachromatic leukodystrophy"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10581",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10581"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:12800",
                        "recommended_name": {
                            "id": "DOID:12800",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:12800",
                            "name": "mucopolysaccharidosis VI",
                            "description": "A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme N-acetylgalactosamine 4-sulfatase."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "MPS VI - Maroteaux-Lamy syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "Maroteaux - Lamy syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "Maroteaux-Lamy syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "arylsulfatase B deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "deficiency of N-acetylgalactosamine-4-sulfatase",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "mucopolysaccharidosis type 6",
                                "description": "Mucopolysaccharidosis type 6 (MPS 6) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate."
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "ARSB deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "ASB deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "MPS6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "MPSVI",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "Maroteaux Lamy Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "Maroteaux-Lamy disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "Maroteaux-Lamy syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "N-acetylgalactosamine 4-sulfatase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "arylsulfatase B deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "mucopolysaccharidosis type VI",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "mucopolysaccharidosis type VI (Maroteaux-Lamy)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "MPS VI",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "Maroteaux Lamy syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "Mucopoly-saccharidosis type VI",
                                "description": ""
                            },
                            {
                                "id": "MIM:253200",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/253200",
                                "name": "Mucopolysaccharidosis 6",
                                "description": "Mucopolysaccharidosis 6"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "12800",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:12800"
                            },
                            {
                                "id": "12800",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:12800"
                            }
                        ]
                    }
                ],
                "filter_code": "000000000000000000100.00000000000000.000000000001000000.00001.11.000.101",
                "uniprot_canonical_ac": "P15848-1"
            },
            {
                "evidence": [
                    {
                        "id": "rs118203944",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs118203944"
                    },
                    {
                        "id": "rs118203944",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs118203944"
                    },
                    {
                        "id": "rs118203944",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs118203944#frequency_tab"
                    },
                    {
                        "id": "rs118203944",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs118203944"
                    },
                    {
                        "id": "8651289",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/8651289"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 393,
                "end_pos": 393,
                "sequence_org": "H",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, arylsulfatase.",
                "chr_id": "5",
                "chr_pos": "78839391",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H393",
                "disease": [
                    {
                        "disease_id": "DOID:12800",
                        "recommended_name": {
                            "id": "DOID:12800",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:12800",
                            "name": "mucopolysaccharidosis VI",
                            "description": "A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme N-acetylgalactosamine 4-sulfatase."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "MPS VI - Maroteaux-Lamy syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "Maroteaux - Lamy syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "Maroteaux-Lamy syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "arylsulfatase B deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:12800",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:12800",
                                "name": "deficiency of N-acetylgalactosamine-4-sulfatase",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "mucopolysaccharidosis type 6",
                                "description": "Mucopolysaccharidosis type 6 (MPS 6) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate."
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "ARSB deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "ASB deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "MPS6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "MPSVI",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009661",
                                "name": "Maroteaux Lamy Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009661",
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                        "field": "total_sites",
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                        "field": "n_linked_glycan_sites",
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        ]
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    {
        "title": "Human ATG3 binding to lipid bilayers: role of lipid geometry, and electric charge.",
        "journal": "Scientific reports",
        "date": "2017",
        "authors": "Hervas JH, Landajuela A, Anton Z, Shnyrova AV, Goni FM, Alonso A",
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            "type": "PubMed",
            "id": "29142222",
            "url": "https://pubmed.ncbi.nlm.nih.gov/29142222"
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                "comment": "Slightly decreases interaction with lipid monolayers; when associated with D-9. Slightly decreases insertion into lipid monolayers; when associated with D-9. Decreases affinity for monolayers containing cardiolipin (CL); when associated with D-9. Cancels selectivity for anionic phospholipids; when associated with D-11. Impairs binding to lipid bilayers; when associated with D-11. Impairs insertion into lipid bilayers; when associated with D-11. Does not induce vesicle tethering; when associated with D-11.",
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                "comment": "Slightly decreases interaction with lipid monolayers; when associated with D-11. Slightly decreases insertion into lipid monolayers; when associated with D-11. Decreases affinity for monolayers containing cardiolipin (CL); when associated with D-11. Cancels selectivity for anionic phospholipids; when associated with D-11. Impairs binding to lipid bilayers; when associated with D-11. Impairs insertion into lipid bilayers; when associated with D-11. Does not induce vesicle tethering; when associated with D-11.",
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        "title": "An N-terminal conserved region in human Atg3 couples membrane curvature sensitivity to conjugase activity during autophagy.",
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        "date": "2021",
        "authors": "Ye Y, Tyndall ER, Bui V, Tang Z, Shen Y, Jiang X, Flanagan JM, Wang HG, Tian F",
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                ],
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                "start_pos": 15,
                "end_pos": 15,
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                "start_pos": 8,
                "end_pos": 8,
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    {
        "title": "Inhibition of ATG3 ameliorates liver steatosis by increasing mitochondrial function.",
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        "authors": "da Silva Lima N, Fondevila MF, Novoa E, Buque X, Mercado-Gomez M, Gallet S, Gonzalez-Rellan MJ, Fernandez U, Loyens A, Garcia-Vence M, Chantada-Vazquez MDP, Bravo SB, Maranon P, Senra A, Escudero A, Leiva M, Guallar D, Fidalgo M, Gomes P, Claret M, Sabio G, Varela-Rey M, Delgado TC, Montero-Vallejo R, Ampuero J, Lopez M, Dieguez C, Herrero L, Serra D, Schwaninger M, Prevot V, Gallego-Duran R, Romero-Gomez M, Iruzubieta P, Crespo J, Martinez-Chantar ML, Garcia-Monzon C, Gonzalez-Rodriguez A, Aspichueta P, Nogueiras R",
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