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- NCIT_C176937 IAO_0000115 "Noonan syndrome caused by autosomal dominant mutation(s) in the SOS2 gene, encoding son of sevenless homolog 2." @default.
- NCIT_C176937 NCIT_A13 NCIT_C177164 @default.
- NCIT_C176937 NCIT_NHC0 "C176937" @default.
- NCIT_C176937 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C176937 NCIT_P108 "Noonan Syndrome 9" @default.
- NCIT_C176937 NCIT_P207 "C4225282" @default.
- NCIT_C176937 NCIT_R176 NCIT_C16612 @default.
- NCIT_C176937 NCIT_R176 NCIT_C177164 @default.
- NCIT_C176937 NCIT_R176 NCIT_C20921 @default.
- NCIT_C176937 normalizedInformationContent "100" @default.
- NCIT_C176937 referenceCount "1" @default.
- NCIT_C176937 hasExactSynonym "NS9" @default.
- NCIT_C176937 hasExactSynonym "Noonan Syndrome 9" @default.
- NCIT_C176937 type Class @default.
- NCIT_C176937 isDefinedBy ncit.owl @default.
- NCIT_C176937 label "Noonan Syndrome 9" @default.
- NCIT_C176937 subClassOf Bbb4f84aca3a539edb3898a4869b04542 @default.
- NCIT_C176937 subClassOf Bda8757fa4fef949537e0eb3730777a88 @default.
- NCIT_C176937 subClassOf NCIT_C176937 @default.
- NCIT_C176937 subClassOf NCIT_C179667 @default.
- NCIT_C176937 subClassOf NCIT_C28193 @default.
- NCIT_C176937 subClassOf NCIT_C2991 @default.
- NCIT_C176937 subClassOf NCIT_C3101 @default.
- NCIT_C176937 subClassOf NCIT_C34854 @default.
- NCIT_C176937 subClassOf NCIT_C7057 @default.