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- NCIT_C179469 IAO_0000115 "An inherited condition caused by mutation(s) in the ALK or PHOX2B genes, encoding ALK tyrosine kinase receptor and paired mesoderm homeobox protein 2B, respectively. The condition is characterized by an increased risk of developing neuroblastoma." @default.
- NCIT_C179469 NCIT_A13 NCIT_C38184 @default.
- NCIT_C179469 NCIT_A13 NCIT_C97724 @default.
- NCIT_C179469 NCIT_NHC0 "C179469" @default.
- NCIT_C179469 NCIT_P106 "Finding" @default.
- NCIT_C179469 NCIT_P108 "Genetic Predisposition to Neuroblastoma" @default.
- NCIT_C179469 NCIT_P208 "CL1662290" @default.
- NCIT_C179469 NCIT_P322 "CCPS" @default.
- NCIT_C179469 normalizedInformationContent "100" @default.
- NCIT_C179469 referenceCount "1" @default.
- NCIT_C179469 hasExactSynonym "Genetic Predisposition to Neuroblastoma" @default.
- NCIT_C179469 inSubset NCIT_C177281 @default.
- NCIT_C179469 inSubset NCIT_C177516 @default.
- NCIT_C179469 type Class @default.
- NCIT_C179469 isDefinedBy ncit.owl @default.
- NCIT_C179469 label "Genetic Predisposition to Neuroblastoma" @default.
- NCIT_C179469 subClassOf NCIT_C171210 @default.
- NCIT_C179469 subClassOf NCIT_C178391 @default.
- NCIT_C179469 subClassOf NCIT_C179469 @default.
- NCIT_C179469 subClassOf NCIT_C3367 @default.
- NCIT_C179469 subClassOf NCIT_C36291 @default.
- NCIT_C179469 subClassOf NCIT_C7057 @default.