Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B34736d05de9be4d05e917d6b3e2400a5> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B34736d05de9be4d05e917d6b3e2400a5 NCIT_P378 "NCI" @default.
- B34736d05de9be4d05e917d6b3e2400a5 type Axiom @default.
- B34736d05de9be4d05e917d6b3e2400a5 annotatedProperty IAO_0000115 @default.
- B34736d05de9be4d05e917d6b3e2400a5 annotatedSource NCIT_C104875 @default.
- B34736d05de9be4d05e917d6b3e2400a5 annotatedTarget "Human CYP26B1 wild-type allele is located in the vicinity of 2p13.2 and is approximately 19 kb in length. This allele, which encodes cytochrome P450 26B1 protein, is involved in the specific inactivation of all-trans-retinoic acid. Mutations in this gene are associated with craniofacial and other skeletal anomalies." @default.