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- Bc0c1af991c8d5a8ddd34f7e9d050be61 NCIT_P378 "NCI" @default.
- Bc0c1af991c8d5a8ddd34f7e9d050be61 NCIT_P381 "EntrezGene" @default.
- Bc0c1af991c8d5a8ddd34f7e9d050be61 type Axiom @default.
- Bc0c1af991c8d5a8ddd34f7e9d050be61 annotatedProperty IAO_0000115 @default.
- Bc0c1af991c8d5a8ddd34f7e9d050be61 annotatedSource NCIT_C97416 @default.
- Bc0c1af991c8d5a8ddd34f7e9d050be61 annotatedTarget "Human CLTCL1 wild-type allele is located in the vicinity of 22q11.2 and is approximately 112 kb in length. This allele, which encodes clathrin heavy chain 2 protein, plays a role in receptor-mediated endocytosis and cellular vesicle transport. Chromosomal aberrations involving this gene are associated with meningioma, DiGeorge syndrome, and velo-cardio-facial syndrome." @default.