Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bb69ada9bcca839033a6378045d68b0c1> ?p ?o ?g. }
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- Bb69ada9bcca839033a6378045d68b0c1 hasDbXref "NCIT:C99022" @default.
- Bb69ada9bcca839033a6378045d68b0c1 type Axiom @default.
- Bb69ada9bcca839033a6378045d68b0c1 annotatedProperty IAO_0000115 @default.
- Bb69ada9bcca839033a6378045d68b0c1 annotatedSource MONDO_0044744 @default.
- Bb69ada9bcca839033a6378045d68b0c1 annotatedTarget "A condition characterized by the congenital or acquired deficiency of prekallikrein. This deficiency is usually not associated with bleeding. The congenital deficiency is very rare. Acquired deficiency may occur in diffuse intravascular coagulation, infections, and sickle cell disease." @default.