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- NCIT_C177534 IAO_0000115 "An autosomal dominant subtype of long QT syndrome caused by mutation(s) in the CALM1 gene, encoding calmodulin-1." @default.
- NCIT_C177534 NCIT_NHC0 "C177534" @default.
- NCIT_C177534 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C177534 NCIT_P108 "Long QT Syndrome 14" @default.
- NCIT_C177534 NCIT_P207 "C4015671" @default.
- NCIT_C177534 NCIT_P322 "Cellosaurus" @default.
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- NCIT_C177534 NCIT_R100 NCIT_C12905 @default.
- NCIT_C177534 NCIT_R100 NCIT_C12919 @default.
- NCIT_C177534 NCIT_R100 NCIT_C13018 @default.
- NCIT_C177534 NCIT_R100 NCIT_C25444 @default.
- NCIT_C177534 NCIT_R176 NCIT_C16612 @default.
- NCIT_C177534 NCIT_R176 NCIT_C21295 @default.
- NCIT_C177534 NCIT_R176 NCIT_C21540 @default.
- NCIT_C177534 normalizedInformationContent "100" @default.
- NCIT_C177534 referenceCount "1" @default.
- NCIT_C177534 hasExactSynonym "LQT14" @default.
- NCIT_C177534 hasExactSynonym "Long QT Syndrome 14" @default.
- NCIT_C177534 inSubset NCIT_C165258 @default.
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- NCIT_C177534 type Class @default.
- NCIT_C177534 isDefinedBy ncit.owl @default.
- NCIT_C177534 label "Long QT Syndrome 14" @default.
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- NCIT_C177534 subClassOf NCIT_C7057 @default.