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- Ba58a54df528e4c5c09fa60b1bb87b6e8 NCIT_P378 "NCI" @default.
- Ba58a54df528e4c5c09fa60b1bb87b6e8 type Axiom @default.
- Ba58a54df528e4c5c09fa60b1bb87b6e8 annotatedProperty IAO_0000115 @default.
- Ba58a54df528e4c5c09fa60b1bb87b6e8 annotatedSource NCIT_C164225 @default.
- Ba58a54df528e4c5c09fa60b1bb87b6e8 annotatedTarget "An autosomal dominant myopathy caused by mutation(s) in the TPM2 gene, encoding tropomyosin beta chain. Classification of nemaline myopathies by clinical features is not optimal, as the phenotypes are highly variable." @default.