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- NCIT_C176938 IAO_0000115 "Noonan syndrome caused by autosomal dominant mutation(s) in the LZTR1 gene, encoding leucine-zipper-like transcriptional regulator 1." @default.
- NCIT_C176938 NCIT_A13 NCIT_C128257 @default.
- NCIT_C176938 NCIT_NHC0 "C176938" @default.
- NCIT_C176938 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176938 NCIT_P108 "Noonan Syndrome 10" @default.
- NCIT_C176938 NCIT_P207 "C4225280" @default.
- NCIT_C176938 NCIT_R176 NCIT_C128257 @default.
- NCIT_C176938 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176938 NCIT_R176 NCIT_C20420 @default.
- NCIT_C176938 NCIT_R176 NCIT_C54362 @default.
- NCIT_C176938 normalizedInformationContent "100" @default.
- NCIT_C176938 referenceCount "1" @default.
- NCIT_C176938 hasExactSynonym "NS10" @default.
- NCIT_C176938 hasExactSynonym "Noonan Syndrome 10" @default.
- NCIT_C176938 type Class @default.
- NCIT_C176938 isDefinedBy ncit.owl @default.
- NCIT_C176938 label "Noonan Syndrome 10" @default.
- NCIT_C176938 subClassOf B310ec57bc28b70e679bde561c6486e08 @default.
- NCIT_C176938 subClassOf Bbc00680ab6cac93e407ec9b2df953d05 @default.
- NCIT_C176938 subClassOf NCIT_C176938 @default.
- NCIT_C176938 subClassOf NCIT_C179667 @default.
- NCIT_C176938 subClassOf NCIT_C28193 @default.
- NCIT_C176938 subClassOf NCIT_C2991 @default.
- NCIT_C176938 subClassOf NCIT_C3101 @default.
- NCIT_C176938 subClassOf NCIT_C34854 @default.
- NCIT_C176938 subClassOf NCIT_C7057 @default.