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- NCIT_C192087 IAO_0000115 "An autosomal dominant form of early infantile epileptic encephalopathy caused by mutation(s) in the KCNQ2 gene, encoding potassium voltage-gated channel subfamily KQT member 2." @default.
- NCIT_C192087 NCIT_NHC0 "C192087" @default.
- NCIT_C192087 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C192087 NCIT_P108 "Developmental and Epileptic Encephalopathy 7" @default.
- NCIT_C192087 NCIT_P207 "C3150986" @default.
- NCIT_C192087 NCIT_P322 "Cellosaurus" @default.
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- NCIT_C192087 NCIT_R100 NCIT_C12438 @default.
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- NCIT_C192087 NCIT_R100 NCIT_C12919 @default.
- NCIT_C192087 NCIT_R100 NCIT_C13040 @default.
- NCIT_C192087 NCIT_R100 NCIT_C32221 @default.
- NCIT_C192087 NCIT_R101 NCIT_C12219 @default.
- NCIT_C192087 NCIT_R101 NCIT_C12439 @default.
- NCIT_C192087 NCIT_R101 NCIT_C13018 @default.
- NCIT_C192087 NCIT_R101 NCIT_C13040 @default.
- NCIT_C192087 NCIT_R101 NCIT_C32221 @default.
- NCIT_C192087 NCIT_R101 NCIT_C33966 @default.
- NCIT_C192087 normalizedInformationContent "100" @default.
- NCIT_C192087 referenceCount "1" @default.
- NCIT_C192087 hasExactSynonym "DEE7" @default.
- NCIT_C192087 hasExactSynonym "Developmental and Epileptic Encephalopathy 7" @default.
- NCIT_C192087 hasExactSynonym "EIEE7" @default.
- NCIT_C192087 hasExactSynonym "Epileptic Encephalopathy, Early Infantile, 7" @default.
- NCIT_C192087 inSubset NCIT_C165258 @default.
- NCIT_C192087 inSubset NCIT_C192842 @default.
- NCIT_C192087 type Class @default.
- NCIT_C192087 isDefinedBy ncit.owl @default.
- NCIT_C192087 label "Developmental and Epileptic Encephalopathy 7" @default.
- NCIT_C192087 subClassOf NCIT_C122814 @default.
- NCIT_C192087 subClassOf NCIT_C192087 @default.
- NCIT_C192087 subClassOf NCIT_C26835 @default.
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- NCIT_C192087 subClassOf NCIT_C27588 @default.
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- NCIT_C192087 subClassOf NCIT_C2991 @default.
- NCIT_C192087 subClassOf NCIT_C53529 @default.
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- NCIT_C192087 subClassOf NCIT_C7057 @default.
- NCIT_C192087 subClassOf NCIT_C96413 @default.
- NCIT_C192087 subClassOf NCIT_C97154 @default.