Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B7bfcc5d908bc7e528097ef6cd03e7c4c> ?p ?o ?g. }
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- B7bfcc5d908bc7e528097ef6cd03e7c4c NCIT_P378 "NCI" @default.
- B7bfcc5d908bc7e528097ef6cd03e7c4c NCIT_P381 "COSMIC" @default.
- B7bfcc5d908bc7e528097ef6cd03e7c4c type Axiom @default.
- B7bfcc5d908bc7e528097ef6cd03e7c4c annotatedProperty IAO_0000115 @default.
- B7bfcc5d908bc7e528097ef6cd03e7c4c annotatedSource NCIT_C97765 @default.
- B7bfcc5d908bc7e528097ef6cd03e7c4c annotatedTarget "Human SNX29 wild-type allele is located in the vicinity of 16p13.13 and is approximately 598 kb in length. This allele, which encodes sorting nexin-29 protein, may play a role in the regulation of GTPase-mediated signaling or lipid trafficking. A point mutation in the gene may be associated with ovarian serous carcinoma." @default.