Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Ba3d46a0175fca8b055d535658dcfd026> ?p ?o ?g. }
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- Ba3d46a0175fca8b055d535658dcfd026 hasDbXref "Orphanet:166078" @default.
- Ba3d46a0175fca8b055d535658dcfd026 type Axiom @default.
- Ba3d46a0175fca8b055d535658dcfd026 annotatedProperty IAO_0000115 @default.
- Ba3d46a0175fca8b055d535658dcfd026 annotatedSource MONDO_0008668 @default.
- Ba3d46a0175fca8b055d535658dcfd026 annotatedTarget "Type 1 von Willebrand disease (type 1 VWD) is a form of VWD characterized by a bleeding disorder associated with a partial quantitative plasmatic deficiency of an otherwise structurally and functionally normal Willebrand factor (von Willebrand factor; VWF)." @default.