Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Be5392ea3f87aaeb24e7301adb447c65b> ?p ?o ?g. }
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- Be5392ea3f87aaeb24e7301adb447c65b hasDbXref "DOID:0060691" @default.
- Be5392ea3f87aaeb24e7301adb447c65b hasDbXref "PMID:18065693" @default.
- Be5392ea3f87aaeb24e7301adb447c65b hasDbXref "PMID:21454453" @default.
- Be5392ea3f87aaeb24e7301adb447c65b hasDbXref "PMID:9834222" @default.
- Be5392ea3f87aaeb24e7301adb447c65b type Axiom @default.
- Be5392ea3f87aaeb24e7301adb447c65b annotatedProperty IAO_0000115 @default.
- Be5392ea3f87aaeb24e7301adb447c65b annotatedSource MONDO_0008552 @default.
- Be5392ea3f87aaeb24e7301adb447c65b annotatedTarget "An inherited blood coagulation disease characterized by autosomal dominant inheritance with macrothrombocytopenia, platelet anisocytosis, prolonged bleeding time but only mildly increased bleeding tendency that has material basis in heterozygous mutation in the ITGA2B gene on chromosome 17q21.31 or the ITGB3 gene on chromosome 17q21.32." @default.