Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bde1d5f7a3df7df8e6dad06da9bdc7a3c> ?p ?o ?g. }
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- Bde1d5f7a3df7df8e6dad06da9bdc7a3c hasDbXref "NCIT:P378" @default.
- Bde1d5f7a3df7df8e6dad06da9bdc7a3c type Axiom @default.
- Bde1d5f7a3df7df8e6dad06da9bdc7a3c annotatedProperty IAO_0000115 @default.
- Bde1d5f7a3df7df8e6dad06da9bdc7a3c annotatedSource MONDO_0005835 @default.
- Bde1d5f7a3df7df8e6dad06da9bdc7a3c 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.