Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B63dda24f682fe1e06ca237cd0b18bc3b> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B63dda24f682fe1e06ca237cd0b18bc3b NCIT_P378 "NCI" @default.
- B63dda24f682fe1e06ca237cd0b18bc3b type Axiom @default.
- B63dda24f682fe1e06ca237cd0b18bc3b annotatedProperty IAO_0000115 @default.
- B63dda24f682fe1e06ca237cd0b18bc3b annotatedSource NCIT_C26721 @default.
- B63dda24f682fe1e06ca237cd0b18bc3b annotatedTarget "An X-linked inherited bleeding disorder caused by deficiency of the coagulation factor IX." @default.