{
    "uniprot_canonical_ac": "Q24535-1",
    "uniprot_ac": "Q24535",
    "uniprot_id": "SRF_DROME",
    "mass": {
        "chemical_mass": 47621.0,
        "monoisotopic_mass": 47621.0
    },
    "refseq": {
        "ac": "NP_001137751",
        "name": "blistered, isoform B",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001137751"
    },
    "gene_names": [
        {
            "name": "bs",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "BS",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "Bs",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "CG3411",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "D-SRF",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "DSRF",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "DSrf",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "DmSRF",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "Dmel\\CG3411",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "Dmel_CG3411",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "Dsrf",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "Group IIc",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "Mal",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "SRF",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "Serf",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "Srf",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "ba; Bs; BS; bs/Dsrf; bs/DSRF; CG3411; D-SRF; Dmel\\CG3411; DmSRF; dsrf; dSRF; DSrf; DSRF; DSrf/bs; Group IIc; l(2)03267; Mal; pruned/DSRF; px; Serf; srf; Srf; SRF",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286837",
            "id": "NP_001286837"
        },
        {
            "name": "ba",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "bs",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286837",
            "id": "NP_001286837"
        },
        {
            "name": "bs",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "dSRF",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "dsrf",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "l(2)03267",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "px",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        },
        {
            "name": "srf",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/Q24535",
            "id": "Q24535"
        }
    ],
    "protein_names": [
        {
            "name": "Serum response factor homolog",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "Q24535"
        },
        {
            "name": "CG3411-PB; bs-PB; drosophila serum response factor; balloon; blistered/DSRF; pruned; SRF; blistered/Drosophila serum response factor",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001137751",
            "id": "NP_001137751"
        },
        {
            "name": "CG3411-PC; bs-PC; drosophila serum response factor; balloon; blistered/DSRF; pruned; SRF; blistered/Drosophila serum response factor",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286837",
            "id": "NP_001286837"
        },
        {
            "name": "Protein blistered",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q24535"
        },
        {
            "name": "blistered, isoform B",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001137751",
            "id": "NP_001137751"
        },
        {
            "name": "blistered, isoform C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286837",
            "id": "NP_001286837"
        },
        {
            "name": "dSRF",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "Q24535"
        }
    ],
    "function": [
        {
            "annotation": "Required for the formation of intervein tissue of the wing. Acts in a dosage-dependent manner to suppress wing vein formation and promote development of intervein cells. Might play a role in the proper formation and maintenance of the trachea.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "Q24535",
                    "url": "https://www.uniprot.org/uniprot/Q24535#function"
                },
                {
                    "database": "PubMed",
                    "id": "8787734",
                    "url": "https://glygen.org/publication/PubMed/8787734"
                },
                {
                    "database": "PubMed",
                    "id": "7600954",
                    "url": "https://glygen.org/publication/PubMed/7600954"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0050700",
            "recommended_name": {
                "id": "DOID:0050700",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050700",
                "name": "cardiomyopathy",
                "description": "A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle."
            },
            "synonyms": [
                {
                    "id": "DOID:0050700",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0050700",
                    "name": "Cardiomyopathies",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "0050700",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050700"
                }
            ]
        },
        {
            "disease_id": "DOID:10763",
            "recommended_name": {
                "id": "DOID:10763",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries."
            },
            "synonyms": [
                {
                    "id": "DOID:10763",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10763",
                    "name": "HTN",
                    "description": ""
                },
                {
                    "id": "DOID:10763",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10763",
                    "name": "hyperpiesia",
                    "description": ""
                },
                {
                    "id": "DOID:10763",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10763",
                    "name": "vascular hypertensive disorder",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "10763",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10763"
                }
            ]
        },
        {
            "disease_id": "DOID:12930",
            "recommended_name": {
                "id": "DOID:12930",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:12930",
                "name": "dilated cardiomyopathy",
                "description": "An intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently."
            },
            "synonyms": [
                {
                    "id": "DOID:12930",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:12930",
                    "name": "primary dilated cardiomyopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "dilated cardiomyopathy 1A",
                    "description": "Familial dilated cardiomyopathy with conduction defect due to LMNA mutation is a rare familial dilated cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy and elevated serum creatine kinase."
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "CDCD1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "LMNA familial isolated dilated cardiomyopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "cardiomyopathy dilated with conduction defect type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "cardiomyopathy, dilated, type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "dilated cardiomyopathy 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "dilated cardiomyopathy type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "dilated cardiomyopathy with conduction defect 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "familial dilated cardiomyopathy with conduction defect due to LMNA mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "familial isolated dilated cardiomyopathy caused by mutation in LMNA",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "cardiomyopathy, congestive",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "cardiomyopathy, dilated, 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "cardiomyopathy, dilated, with conduction defect 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "cardiomyopathy, familial idiopathic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007269",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007269",
                    "name": "cardiomyopathy, idiopathic dilated",
                    "description": ""
                },
                {
                    "id": "MIM:115200",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/115200",
                    "name": "Cardiomyopathy, dilated, 1A",
                    "description": "Cardiomyopathy, dilated, 1A"
                }
            ],
            "evidence": [
                {
                    "id": "12930",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:12930"
                }
            ]
        },
        {
            "disease_id": "DOID:3319",
            "recommended_name": {
                "id": "DOID:3319",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3319",
                "name": "lymphangioleiomyomatosis",
                "description": "A lung disease that is characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas."
            },
            "synonyms": [
                {
                    "id": "DOID:3319",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3319",
                    "name": "lung lymphangioleiomyomatosis",
                    "description": ""
                },
                {
                    "id": "DOID:3319",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3319",
                    "name": "lymphangiomyomatosis",
                    "description": ""
                },
                {
                    "id": "DOID:3319",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3319",
                    "name": "pulmonary lymphangioleiomyomatosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011705",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011705",
                    "name": "lymphangioleiomyomatosis",
                    "description": "A multifocal neoplasm with perivascular epithelioid cell differentiation affecting almost exclusively females of child-bearing age. It is characterized by the presence of smooth muscle and epithelioid cells and by the proliferation of lymphatic vessels. Sites of involvement include the lungs, mediastinum, and the retroperitoneum. It usually presents with chylous pleural effusion or ascites."
                },
                {
                    "id": "MONDO:0011705",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011705",
                    "name": "lymphangioleiomyomatosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011705",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011705",
                    "name": "lymphangioleiomyomatosis, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0011705",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011705",
                    "name": "lymphangiomyomatosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011705",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011705",
                    "name": "lung lymphangioleiomyomatosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011705",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011705",
                    "name": "pulmonary lymphangioleiomyomatosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011705",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011705",
                    "name": "LAM",
                    "description": ""
                },
                {
                    "id": "MONDO:0011705",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011705",
                    "name": "lymphangio-myomatosis",
                    "description": ""
                },
                {
                    "id": "MIM:606690",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/606690",
                    "name": "Lymphangioleiomyomatosis",
                    "description": "Lymphangioleiomyomatosis"
                }
            ],
            "evidence": [
                {
                    "id": "3319",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3319"
                }
            ]
        },
        {
            "disease_id": "DOID:6000",
            "recommended_name": {
                "id": "DOID:6000",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body."
            },
            "synonyms": [
                {
                    "id": "DOID:6000",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:6000",
                    "name": "CHF",
                    "description": ""
                },
                {
                    "id": "DOID:6000",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:6000",
                    "name": "Cardiac Failure Congestive",
                    "description": ""
                },
                {
                    "id": "DOID:6000",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:6000",
                    "name": "Congestive heart disease",
                    "description": ""
                },
                {
                    "id": "DOID:6000",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:6000",
                    "name": "Weak heart",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "6000",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:6000"
                }
            ]
        },
        {
            "disease_id": "DOID:684",
            "recommended_name": {
                "id": "DOID:684",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver."
            },
            "synonyms": [
                {
                    "id": "DOID:684",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:684",
                    "name": "Hepatoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma",
                    "description": "A malignant tumor that arises from hepatocytes. Hepatocellular carcinoma is relatively rare in the United States but very common in all African countries south of the Sahara and in Southeast Asia. Most cases are seen in patients over the age of 50 years, but this tumor can also occur in younger individuals and even in children. Hepatocellular carcinoma is more common in males than females and is associated with hepatitis B, hepatitis C, chronic alcohol abuse and cirrhosis. Serum elevation of alpha-fetoprotein occurs in a large percentage of patients with hepatocellular carcinoma. Grossly, hepatocellular carcinoma may present as a single mass, as multiple nodules, or as diffuse liver involvement. Microscopically, there is a wide range of differentiation from tumor to tumor (well differentiated to poorly differentiated tumors). Hepatocellular carcinomas quickly metastasize to regional lymph nodes and lung. The overall median survival of untreated liver cell carcinoma is about 4 months. The most effective treatment of hepatocellular carcinoma is complete resection of the tumor. Lately, an increasing number of tumors have been treated with liver transplantation."
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "HCC",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "cancer, hepatocellular",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma of liver",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma of liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma of the liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "carcinoma, hepatocellular, malignant",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoblastoma, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular adenocarcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular cancer, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma, childhood type, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoma",
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                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver cell cancer (hepatocellular carcinoma)",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver cell carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "primary carcinoma of liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "primary carcinoma of the liver cells",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "adult hepatoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "adult primary hepatocellular carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoblastoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatoblastoma caused by somatic mutation",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver and intrahepatic bile duct carcinoma",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "liver cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
                    "name": "hepatocellular carcinoma",
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                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
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                    "description": ""
                },
                {
                    "id": "MONDO:0007256",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
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                },
                {
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                },
                {
                    "id": "MONDO:0007256",
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                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
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                },
                {
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                },
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                },
                {
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                },
                {
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                },
                {
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                    "url": "https://monarchinitiative.org/disease/MONDO:0007256",
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                },
                {
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                },
                {
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                },
                {
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                },
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            "database": "InterPro",
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            "id": "IPR033897",
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            "kinase_gene_name": "",
            "residue": "Ser",
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