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- B87618a14c013659d594428787d65342c NCIT_P378 "NICHD" @default.
- B87618a14c013659d594428787d65342c type Axiom @default.
- B87618a14c013659d594428787d65342c annotatedProperty NCIT_P325 @default.
- B87618a14c013659d594428787d65342c annotatedSource NCIT_C3225 @default.
- B87618a14c013659d594428787d65342c annotatedTarget "Multiple endocrine neoplasia caused by inactivating mutation(s) of the tumor suppressor gene MEN1, encoding the menin protein, a component of the histone methyltransferase complex. The condition is characterized by hyperfunctioning adenomas of the parathyroid glands, adrenal glands, pituitary gland, and pancreatic endocrine cells (most commonly gastrinomas and insulinomas); thymic and bronchial carcinoid tumors also may develop." @default.