[
    {
        "title": "G Protein-coupled receptor kinases phosphorylate LRP6 in the Wnt pathway.",
        "journal": "J. Biol. Chem.",
        "date": "2009",
        "authors": "Chen M, Philipp M, Wang J, Premont RT, Garrison TR, Caron MG, Lefkowitz RJ, Chen W",
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                "protein_name": "Forkhead box protein D3",
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        "record_id": "pubmed.9845073",
        "abstract": "",
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    },
    {
        "title": "Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of alpha-dystroglycan.",
        "journal": "Am. J. Hum. Genet.",
        "date": "2013",
        "authors": "Carss KJ, Stevens E, Foley AR, Cirak S, Riemersma M, Torelli S, Hoischen A, Willer T, van Scherpenzeel M, Moore SA, Messina S, Bertini E, Bonnemann CG, Abdenur JE, Grosmann CM, Kesari A, Punetha J, Quinlivan R, Waddell LB, Young HK, Wraige E, Yau S, Brodd L, Feng L, Sewry C, MacArthur DG, North KN, Hoffman E, Stemple DL, Hurles ME, van Bokhoven H, Campbell KP, Lefeber DJ, Lin YY, Muntoni F",
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                "tax_name": "Zebrafish"
            },
            {
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                "protein_name": "Mannose-1-phosphate guanylyltransferase catalytic subunit beta",
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            }
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                ],
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                "glygen_name": "Zebrafish",
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        ],
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                    {
                        "id": "rs397509425",
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                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs397509425"
                    },
                    {
                        "id": "rs397509425",
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                    {
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                ],
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                            {
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                            {
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                            {
                                "id": "DOID:0110294",
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                            {
                                "id": "DOID:0110294",
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014142",
                                "name": "autosomal recessive limb-girdle muscular dystrophy type 2T",
                                "description": "Autosomal recessive limb-girdle muscular dystrophy type 2T (LGMD2T) is a form of limb-girdle muscular dystrophy, that can present from birth to early childhood, characterized by hypotonia, microcephaly, mild proximal muscle weakness (leading to delayed walking and difficulty climbing stairs), mild intellectual disability and epilepsy. Additional manifestations reported in some patients include cataracts, nystagmus, cardiomyopathy, and respiratory insufficiency."
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                            {
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                            {
                                "id": "MONDO:0014142",
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                                "id": "MONDO:0014142",
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                            {
                                "id": "MONDO:0014142",
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                            {
                                "id": "MONDO:0014142",
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                                "description": "Muscular dystrophy-dystroglycanopathy limb-girdle C14"
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                    {
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                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111233",
                            "name": "congenital muscular dystrophy-dystroglycanopathy type A14",
                            "description": "A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in in GMPPB on 3p21.31."
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                                "id": "DOID:0111233",
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                                "url": "https://disease-ontology.org/term/DOID:0111233",
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                                "description": ""
                            },
                            {
                                "id": "DOID:0111233",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111233",
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                                "description": ""
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                            {
                                "id": "DOID:0111233",
                                "resource": "Disease Ontology",
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                                "name": "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014140",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014140",
                                "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14",
                                "description": ""
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                            {
                                "id": "MONDO:0014140",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014140",
                                "name": "muscle-eye-brain-GMPPB related",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014140",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0014140",
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                            {
                                "id": "MONDO:0014140",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014140",
                                "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14",
                                "description": ""
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                            {
                                "id": "MIM:615350",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/615350",
                                "name": "Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A14",
                                "description": "Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A14"
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                                "id": "0014140",
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                                "id": "615350",
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                        },
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                                "id": "DOID:0112377",
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                                "name": "congenital muscular dystrophy GMPPB-related",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0014141",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014141",
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                            {
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                            {
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                            {
                                "id": "MONDO:0014141",
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                                "name": "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 14",
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                            {
                                "id": "MONDO:0014141",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014141",
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                                "id": "MIM:615351",
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                                "url": "https://www.omim.org/entry/615351",
                                "name": "Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B14",
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                                "id": "DOID:0110294",
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                                "description": ""
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                            {
                                "id": "DOID:0110294",
                                "resource": "Disease Ontology",
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                                "name": "MDDGC14",
                                "description": ""
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                            {
                                "id": "DOID:0110294",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110294",
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                                "description": ""
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                            {
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                        ]
                    },
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                            "id": "DOID:0111233",
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                            {
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                            {
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                            {
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                            {
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                            "id": "DOID:0112377",
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                            {
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