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- Bb324f04221635dd01748d1b9018b825d NCIT_P378 "NICHD" @default.
- Bb324f04221635dd01748d1b9018b825d type Axiom @default.
- Bb324f04221635dd01748d1b9018b825d annotatedProperty NCIT_P325 @default.
- Bb324f04221635dd01748d1b9018b825d annotatedSource NCIT_C3225 @default.
- Bb324f04221635dd01748d1b9018b825d 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.