Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B211841da21f4b15a8c0ac3bf22fbb843> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B211841da21f4b15a8c0ac3bf22fbb843 NCIT_P378 "NCI" @default.
- B211841da21f4b15a8c0ac3bf22fbb843 type Axiom @default.
- B211841da21f4b15a8c0ac3bf22fbb843 annotatedProperty IAO_0000115 @default.
- B211841da21f4b15a8c0ac3bf22fbb843 annotatedSource NCIT_C155998 @default.
- B211841da21f4b15a8c0ac3bf22fbb843 annotatedTarget "An autosomal dominant form of early infantile epileptic encephalopathy, caused by mutation(s) in the KCNA2 gene, encoding potassium voltage-gated channel subfamily A member 2." @default.