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                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
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                        "count": 0
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                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
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                    {
                        "field": "o_linked_glycans",
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                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Old gene, new phenotype: mutations in heparan sulfate synthesis enzyme, EXT2 leads to seizure and developmental disorder, no exostoses.",
        "journal": "Journal of medical genetics",
        "date": "2015",
        "authors": "Farhan SM, Wang J, Robinson JF, Prasad AN, Rupar CA, Siu VM, Hegele RA",
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            "type": "PubMed",
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            {
                "uniprot_canonical_ac": "Q93063-1",
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        ],
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            {
                "name": "Homo sapiens",
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                    {
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                ],
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        ],
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            {
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                    {
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                    {
                        "id": "rs140075817",
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                    {
                        "id": "rs140075817",
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                    {
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                ],
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                            {
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                            {
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                            {
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                            {
                                "id": "DOID:206",
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                            {
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                            {
                                "id": "MONDO:0007585",
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                            {
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                            {
                                "id": "MONDO:0007585",
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                            {
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                            {
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                            {
                                "id": "MONDO:0007586",
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                                "id": "MONDO:0007586",
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                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
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                            {
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                                "id": "DOID:1319",
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                            {
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                                "resource": "Disease Ontology",
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                            {
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                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
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                            {
                                "id": "DOID:1319",
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                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
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                                "description": ""
                            }
                        ],
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                            "DOID:3541",
                            "DOID:4706",
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                            {
                                "id": "DOID:206",
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                                "description": ""
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                            {
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                            {
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                            {
                                "id": "DOID:206",
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                            {
                                "id": "DOID:206",
                                "resource": "Disease Ontology",
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                                "description": ""
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                            {
                                "id": "MONDO:0007585",
                                "resource": "MONDO",
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                            },
                            {
                                "id": "MONDO:0007585",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007585",
                                "name": "EXT1 exostoses, multiple",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007585",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007585",
                                "name": "exostoses, multiple caused by mutation in EXT1",
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                            {
                                "id": "MONDO:0007585",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007585",
                                "name": "exostoses, multiple, type 1",
                                "description": ""
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                            {
                                "id": "MONDO:0007585",
                                "resource": "MONDO",
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                                "name": "EXT",
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                            },
                            {
                                "id": "MONDO:0007586",
                                "resource": "MONDO",
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                            },
                            {
                                "id": "MONDO:0007586",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007586",
                                "name": "EXT2 Gene",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007586",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007586",
                                "name": "EXT2 exostoses, multiple",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007586",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007586",
                                "name": "exostoses (Multiple) 2 Gene",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007586",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007586",
                                "name": "exostoses, multiple caused by mutation in EXT2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007586",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007586",
                                "name": "exostoses, multiple, type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010846",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010846",
                                "name": "exostoses, multiple, type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010846",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010846",
                                "name": "EXT3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010846",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010846",
                                "name": "exostoses, multiple, type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010846",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010846",
                                "name": "exostoses, multiple, type 3",
                                "description": ""
                            },
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    {
        "title": "Novel exostosin-2 missense variants in a family with autosomal recessive exostosin-2-related syndrome: further evidences on the phenotype.",
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        "date": "2019",
        "authors": "Gentile M, Agolini E, Cocciadiferro D, Ficarella R, Ponzi E, Bellacchio E, Antonucci MF, Novelli A",
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