Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Be05de7d2d407e715dbc790186b630c92> ?p ?o ?g. }
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- Be05de7d2d407e715dbc790186b630c92 NCIT_P378 "NCI" @default.
- Be05de7d2d407e715dbc790186b630c92 type Axiom @default.
- Be05de7d2d407e715dbc790186b630c92 annotatedProperty IAO_0000115 @default.
- Be05de7d2d407e715dbc790186b630c92 annotatedSource NCIT_C172092 @default.
- Be05de7d2d407e715dbc790186b630c92 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.