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- Bf826f02bba12af9c34f05fbaeb67d618 NCIT_P378 "NCI" @default.
- Bf826f02bba12af9c34f05fbaeb67d618 type Axiom @default.
- Bf826f02bba12af9c34f05fbaeb67d618 annotatedProperty IAO_0000115 @default.
- Bf826f02bba12af9c34f05fbaeb67d618 annotatedSource NCIT_C172092 @default.
- Bf826f02bba12af9c34f05fbaeb67d618 annotatedTarget "An autosomal dominant subtype of familial hypertrophic cardiomyopathy caused by mutation(s) in the CAV3 gene, MYH7 gene, or MYLK2 gene encoding caveolin-3, myosin heavy chain 7, and myosin light chain kinase 2, skeletal/cardiac muscle respectively." @default.