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- NCIT_C164225 IAO_0000115 "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.
- NCIT_C164225 NCIT_NHC0 "C164225" @default.
- NCIT_C164225 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C164225 NCIT_P108 "Nemaline Myopathy 4" @default.
- NCIT_C164225 NCIT_P207 "C1836447" @default.
- NCIT_C164225 NCIT_P322 "Cellosaurus" @default.
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- NCIT_C164225 NCIT_R103 NCIT_C12219 @default.
- NCIT_C164225 NCIT_R103 NCIT_C12471 @default.
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- NCIT_C164225 NCIT_R135 NCIT_C12219 @default.
- NCIT_C164225 NCIT_R135 NCIT_C12366 @default.
- NCIT_C164225 NCIT_R135 NCIT_C25769 @default.
- NCIT_C164225 NCIT_R135 NCIT_C32221 @default.
- NCIT_C164225 NCIT_R135 NCIT_C34076 @default.
- NCIT_C164225 NCIT_R176 NCIT_C115001 @default.
- NCIT_C164225 NCIT_R176 NCIT_C16612 @default.
- NCIT_C164225 NCIT_R176 NCIT_C20744 @default.
- NCIT_C164225 NCIT_R176 NCIT_C20745 @default.
- NCIT_C164225 normalizedInformationContent "100" @default.
- NCIT_C164225 referenceCount "1" @default.
- NCIT_C164225 hasExactSynonym "NEM4" @default.
- NCIT_C164225 hasExactSynonym "Nemaline Myopathy 4" @default.
- NCIT_C164225 inSubset NCIT_C165258 @default.
- NCIT_C164225 inSubset NCIT_C192842 @default.
- NCIT_C164225 type Class @default.
- NCIT_C164225 isDefinedBy ncit.owl @default.
- NCIT_C164225 label "Nemaline Myopathy 4" @default.
- NCIT_C164225 subClassOf B5740949cae7aa0ccf2feb45f99115bdf @default.
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- NCIT_C164225 subClassOf NCIT_C166355 @default.
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- NCIT_C164225 subClassOf NCIT_C7057 @default.