Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bd3b1085d7b23cf9a47a62457edc95b54> ?p ?o ?g. }
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- Bd3b1085d7b23cf9a47a62457edc95b54 hasDbXref "NCIT:C99022" @default.
- Bd3b1085d7b23cf9a47a62457edc95b54 type Axiom @default.
- Bd3b1085d7b23cf9a47a62457edc95b54 annotatedProperty IAO_0000115 @default.
- Bd3b1085d7b23cf9a47a62457edc95b54 annotatedSource MONDO_0044744 @default.
- Bd3b1085d7b23cf9a47a62457edc95b54 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.