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- Bd29a234db16f8b62dc166206b28e2dd1 NCIT_P378 "NCI" @default.
- Bd29a234db16f8b62dc166206b28e2dd1 type Axiom @default.
- Bd29a234db16f8b62dc166206b28e2dd1 annotatedProperty IAO_0000115 @default.
- Bd29a234db16f8b62dc166206b28e2dd1 annotatedSource NCIT_C8494 @default.
- Bd29a234db16f8b62dc166206b28e2dd1 annotatedTarget "An autosomal dominant hereditary neoplastic syndrome characterized by the development of colorectal carcinoma and a high risk of developing endometrial carcinoma, gastric carcinoma, ovarian carcinoma, renal pelvis carcinoma, and small intestinal carcinoma. Patients often develop colorectal carcinomas at an early age (mean, 45 years). In the majority of the cases the lesions arise from the proximal colon. At the molecular level, high-frequency microsatellite instability is present." @default.