Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bc6382f5cd4302a14fa0d859b86769665> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bc6382f5cd4302a14fa0d859b86769665 hasDbXref "Orphanet:325" @default.
- Bc6382f5cd4302a14fa0d859b86769665 type Axiom @default.
- Bc6382f5cd4302a14fa0d859b86769665 annotatedProperty IAO_0000115 @default.
- Bc6382f5cd4302a14fa0d859b86769665 annotatedSource MONDO_0013361 @default.
- Bc6382f5cd4302a14fa0d859b86769665 annotatedTarget "Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms." @default.