Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B0e14d392c921a722b723f44ac6e8be3a> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B0e14d392c921a722b723f44ac6e8be3a NCIT_P378 "NCI" @default.
- B0e14d392c921a722b723f44ac6e8be3a type Axiom @default.
- B0e14d392c921a722b723f44ac6e8be3a annotatedProperty IAO_0000115 @default.
- B0e14d392c921a722b723f44ac6e8be3a annotatedSource NCIT_C178648 @default.
- B0e14d392c921a722b723f44ac6e8be3a annotatedTarget "Human CFB wild-type allele is located in the vicinity of 6p21.33 and is approximately 6 kb in length. This allele, which encodes complement factor B protein, is involved in convertase activity associated with complement activation. Mutation of the gene is associated with complement deficiency, decreased risk for age-related macular degeneration and increased susceptibility to atypical hemolytic uremic syndrome." @default.