Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B33663ef4032bc5e02bf353b684330600> ?p ?o ?g. }
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- B33663ef4032bc5e02bf353b684330600 NCIT_P378 "NCI" @default.
- B33663ef4032bc5e02bf353b684330600 type Axiom @default.
- B33663ef4032bc5e02bf353b684330600 annotatedProperty IAO_0000115 @default.
- B33663ef4032bc5e02bf353b684330600 annotatedSource NCIT_C133725 @default.
- B33663ef4032bc5e02bf353b684330600 annotatedTarget "An autosomal dominant condition caused by mutation(s) in the MYBPC3 gene, encoding MYBPC3 protein. It is characterized by severe neonatal hypertrophic cardiomyopathy." @default.