Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B0caf3268873788da03a973fab98c22a7> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B0caf3268873788da03a973fab98c22a7 NCIT_P378 "NCI" @default.
- B0caf3268873788da03a973fab98c22a7 type Axiom @default.
- B0caf3268873788da03a973fab98c22a7 annotatedProperty IAO_0000115 @default.
- B0caf3268873788da03a973fab98c22a7 annotatedSource NCIT_C189277 @default.
- B0caf3268873788da03a973fab98c22a7 annotatedTarget "An autosomal dominant subtype of familial hemiplegic migraine caused by mutation(s) in the CACNA1A gene, encoding voltage-dependent P/Q-type calcium channel subunit alpha-1A." @default.