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- NCIT_C157266 IAO_0000115 "An autosomal dominant sub-type of left ventricular noncompaction syndrome caused by heterozygous mutation(s) of the MIB1 gene, encoding E3 ubiquitin-protein ligase MIB1." @default.
- NCIT_C157266 NCIT_NHC0 "C157266" @default.
- NCIT_C157266 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C157266 NCIT_P108 "Left Ventricular Noncompaction 7" @default.
- NCIT_C157266 NCIT_P207 "C3554496" @default.
- NCIT_C157266 NCIT_P322 "Cellosaurus" @default.
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- NCIT_C157266 NCIT_R100 NCIT_C12905 @default.
- NCIT_C157266 NCIT_R100 NCIT_C12919 @default.
- NCIT_C157266 NCIT_R100 NCIT_C13018 @default.
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- NCIT_C157266 NCIT_R176 NCIT_C104651 @default.
- NCIT_C157266 NCIT_R176 NCIT_C133710 @default.
- NCIT_C157266 NCIT_R176 NCIT_C16612 @default.
- NCIT_C157266 NCIT_R176 NCIT_C21281 @default.
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- NCIT_C157266 normalizedInformationContent "100" @default.
- NCIT_C157266 referenceCount "1" @default.
- NCIT_C157266 hasExactSynonym "LVNC7" @default.
- NCIT_C157266 hasExactSynonym "Left Ventricular Noncompaction 7" @default.
- NCIT_C157266 inSubset NCIT_C165258 @default.
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- NCIT_C157266 type Class @default.
- NCIT_C157266 isDefinedBy ncit.owl @default.
- NCIT_C157266 label "Left Ventricular Noncompaction 7" @default.
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