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- B27e04b3fed044889b8dc0d806ce2ac2e hasDbXref "NCIT:C133725" @default.
- B27e04b3fed044889b8dc0d806ce2ac2e type Axiom @default.
- B27e04b3fed044889b8dc0d806ce2ac2e annotatedProperty IAO_0000115 @default.
- B27e04b3fed044889b8dc0d806ce2ac2e annotatedSource MONDO_0007268 @default.
- B27e04b3fed044889b8dc0d806ce2ac2e 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.