Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B2913a032abd82259b7ca22e94413b0e2> ?p ?o ?g. }
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- B2913a032abd82259b7ca22e94413b0e2 NCIT_P378 "NCI" @default.
- B2913a032abd82259b7ca22e94413b0e2 type Axiom @default.
- B2913a032abd82259b7ca22e94413b0e2 annotatedProperty IAO_0000115 @default.
- B2913a032abd82259b7ca22e94413b0e2 annotatedSource NCIT_C93102 @default.
- B2913a032abd82259b7ca22e94413b0e2 annotatedTarget "A genetic variation that is known to be associated with an increased risk of disease." @default.