Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5e759f526235b0ab62848d0abd82d88b> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B5e759f526235b0ab62848d0abd82d88b hasDbXref "Orphanet:328" @default.
- B5e759f526235b0ab62848d0abd82d88b type Axiom @default.
- B5e759f526235b0ab62848d0abd82d88b annotatedProperty IAO_0000115 @default.
- B5e759f526235b0ab62848d0abd82d88b annotatedSource MONDO_0009212 @default.
- B5e759f526235b0ab62848d0abd82d88b annotatedTarget "Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms." @default.