Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B07d26ac5f0194efd1cca08d1cecb31d3> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B07d26ac5f0194efd1cca08d1cecb31d3 NCIT_P378 "NCI" @default.
- B07d26ac5f0194efd1cca08d1cecb31d3 type Axiom @default.
- B07d26ac5f0194efd1cca08d1cecb31d3 annotatedProperty IAO_0000115 @default.
- B07d26ac5f0194efd1cca08d1cecb31d3 annotatedSource NCIT_C75508 @default.
- B07d26ac5f0194efd1cca08d1cecb31d3 annotatedTarget "Human HIRA wild-type allele is located in the vicinity of 22q11.2 or 22q11.21 and is approximately 101 kb in length. This allele, which encodes protein HIRA, is involved in the modulation of chromatin structure. Haploinsufficiency of the gene may be a factor in DiGeorge syndrome." @default.