Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B6cf55b1076bf82dc96d0f3e24e61b4b2> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B6cf55b1076bf82dc96d0f3e24e61b4b2 NCIT_P378 "NCI" @default.
- B6cf55b1076bf82dc96d0f3e24e61b4b2 type Axiom @default.
- B6cf55b1076bf82dc96d0f3e24e61b4b2 annotatedProperty IAO_0000115 @default.
- B6cf55b1076bf82dc96d0f3e24e61b4b2 annotatedSource NCIT_C189273 @default.
- B6cf55b1076bf82dc96d0f3e24e61b4b2 annotatedTarget "An autosomal recessive subtype of developmental and epileptic encephalopathy caused by mutation(s) in the WWOX gene, encoding WW domain-containing oxidoreductase." @default.