Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8c5829f3baf8df8d867061564a0a1280> ?p ?o ?g. }
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- B8c5829f3baf8df8d867061564a0a1280 hasDbXref "Orphanet:36355" @default.
- B8c5829f3baf8df8d867061564a0a1280 type Axiom @default.
- B8c5829f3baf8df8d867061564a0a1280 annotatedProperty IAO_0000115 @default.
- B8c5829f3baf8df8d867061564a0a1280 annotatedSource MONDO_0012354 @default.
- B8c5829f3baf8df8d867061564a0a1280 annotatedTarget "P2Y12 defect is a rare hemorrhagic disorder characterized by mild to moderate bleeding diathesis with easy bruising, mucosal bleedings, and excessive post-operative hemorrhage due to defect of the platelet P2Y12 receptor resulting in selective impairment of platelet responses to adenosine diphosphate." @default.