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    {
        "title": "Isolation of cDNA clones encoding eight different human G protein gamma subunits, including three novel forms designated the gamma 4, gamma 10, and gamma 11 subunits.",
        "journal": "The Journal of biological chemistry",
        "date": "1995",
        "authors": "Ray K, Kunsch C, Bonner LM, Robishaw JD",
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                ],
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        ],
        "record_id": "pubmed.7665596",
        "abstract": "",
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            {
                "table_id": "referenced_proteins",
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    {
        "title": "Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene.",
        "journal": "Human molecular genetics",
        "date": "2000",
        "authors": "Veugelers M, Cat BD, Muyldermans SY, Reekmans G, Delande N, Frints S, Legius E, Fryns JP, Schrander-Stumpel C, Weidle B, Magdalena N, David G",
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                ],
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                            {
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                            {
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                                "resource": "Disease Ontology",
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                            {
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                                "name": "breast cancer, early-onset, susceptibility to, autosomal dominant, somatic mutation",
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                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, invasive ductal, autosomal dominant, somatic mutation",
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                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, lobular, somatic",
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                                "id": "MONDO:0016419",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, male, susceptibility to, autosomal dominant, somatic mutation",
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                                "id": "MONDO:0016419",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, protection against, autosomal dominant, somatic mutation",
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                                "name": "breast cancer, somatic",
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                                "id": "MONDO:0016419",
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                                "name": "breast cancer, susceptibility to, autosomal dominant, somatic mutation",
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                                "id": "MONDO:0016419",
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                                "id": "MONDO:0016419",
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                                "name": "Breast cancer",
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                    {
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                            "url": "https://disease-ontology.org/term/DOID:0060248",
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                            "description": "A syndrome characterized by pre- and postnatal overgrowth and craniofacial, skeletal, cardiac and renal abnormalities and has_material_basis_in mutation in the gene encoding glypican-3 (GPC3) on chromosome Xq26."
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                            {
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                                "description": ""
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                            {
                                "id": "DOID:0060248",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0060248",
                                "name": "SGB syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0060248",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0060248",
                                "name": "Sara Angers syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0060248",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0060248",
                                "name": "Simpson dysmorphia syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0060248",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0060248",
                                "name": "X-linked dysplasia gigantism syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0060248",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0060248",
                                "name": "bulldog syndrome",
                                "description": ""
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                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0020602",
                                "name": "Simpson-Golabi-Behmel syndrome type 1",
                                "description": "Any Simpson-Golabi-Behmel syndrome in which the cause of the disease is a mutation in the GPC3 gene."
                            },
                            {
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    {
        "title": "The Simpson-Golabi-Behmel syndrome causative glypican-3, binds to and inhibits the dipeptidyl peptidase activity of CD26.",
        "journal": "Proteomics",
        "date": "2007",
        "authors": "Davoodi J, Kelly J, Gendron NH, MacKenzie AE",
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    {
        "title": "Germinal mosaicism in Simpson-Golabi-Behmel syndrome.",
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        "authors": "Romanelli V, Arroyo I, Rodriguez J I, Magano L, Arias P, Incera I, Gracia-Bouthelier R, Lapunzina P",
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        "authors": "Peng Jin, Zhang Qingfeng, Lin Fei, Ke Chao, Deng Wuguo, Yang Ankui, Su Xuan",
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            "id": "37990886",
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        "abstract": "",
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