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- NCIT_C192202 IAO_0000115 "An autosomal dominant subtype of long QT syndrome caused by mutation(s) in the SNTA1 gene, encoding alpha-1-syntrophin." @default.
- NCIT_C192202 NCIT_NHC0 "C192202" @default.
- NCIT_C192202 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C192202 NCIT_P108 "Long QT Syndrome 12" @default.
- NCIT_C192202 NCIT_P207 "C2751830" @default.
- NCIT_C192202 NCIT_P322 "Cellosaurus" @default.
- NCIT_C192202 NCIT_R100 NCIT_C12219 @default.
- NCIT_C192202 NCIT_R100 NCIT_C12686 @default.
- NCIT_C192202 NCIT_R100 NCIT_C12727 @default.
- NCIT_C192202 NCIT_R100 NCIT_C12779 @default.
- NCIT_C192202 NCIT_R100 NCIT_C12905 @default.
- NCIT_C192202 NCIT_R100 NCIT_C12919 @default.
- NCIT_C192202 NCIT_R100 NCIT_C13018 @default.
- NCIT_C192202 NCIT_R100 NCIT_C25444 @default.
- NCIT_C192202 normalizedInformationContent "100" @default.
- NCIT_C192202 referenceCount "1" @default.
- NCIT_C192202 hasExactSynonym "LQT12" @default.
- NCIT_C192202 hasExactSynonym "Long QT Syndrome 12" @default.
- NCIT_C192202 inSubset NCIT_C165258 @default.
- NCIT_C192202 inSubset NCIT_C192842 @default.
- NCIT_C192202 type Class @default.
- NCIT_C192202 isDefinedBy ncit.owl @default.
- NCIT_C192202 label "Long QT Syndrome 12" @default.
- NCIT_C192202 subClassOf NCIT_C192202 @default.
- NCIT_C192202 subClassOf NCIT_C27551 @default.
- NCIT_C192202 subClassOf NCIT_C27669 @default.
- NCIT_C192202 subClassOf NCIT_C27672 @default.
- NCIT_C192202 subClassOf NCIT_C28193 @default.
- NCIT_C192202 subClassOf NCIT_C2931 @default.
- NCIT_C192202 subClassOf NCIT_C2991 @default.
- NCIT_C192202 subClassOf NCIT_C3079 @default.
- NCIT_C192202 subClassOf NCIT_C34786 @default.
- NCIT_C192202 subClassOf NCIT_C35741 @default.
- NCIT_C192202 subClassOf NCIT_C35742 @default.
- NCIT_C192202 subClassOf NCIT_C35743 @default.
- NCIT_C192202 subClassOf NCIT_C53529 @default.
- NCIT_C192202 subClassOf NCIT_C53531 @default.
- NCIT_C192202 subClassOf NCIT_C7057 @default.