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- NCIT_C175955 IAO_0000115 "A cytogenetic abnormality that refers to the duplication of all or part of the long arm of chromosome 16." @default.
- NCIT_C175955 NCIT_NHC0 "C175955" @default.
- NCIT_C175955 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C175955 NCIT_P108 "Gain of Chromosome 16q" @default.
- NCIT_C175955 NCIT_P208 "CL1413133" @default.
- NCIT_C175955 NCIT_R173 NCIT_C12219 @default.
- NCIT_C175955 NCIT_R173 NCIT_C13202 @default.
- NCIT_C175955 NCIT_R173 NCIT_C13203 @default.
- NCIT_C175955 NCIT_R173 NCIT_C13211 @default.
- NCIT_C175955 NCIT_R173 NCIT_C13404 @default.
- NCIT_C175955 NCIT_R173 NCIT_C14134 @default.
- NCIT_C175955 NCIT_R173 NCIT_C21599 @default.
- NCIT_C175955 normalizedInformationContent "100" @default.
- NCIT_C175955 referenceCount "1" @default.
- NCIT_C175955 hasExactSynonym "Gain of Chromosome 16q" @default.
- NCIT_C175955 hasExactSynonym "add(16q)" @default.
- NCIT_C175955 type Class @default.
- NCIT_C175955 isDefinedBy ncit.owl @default.
- NCIT_C175955 label "Gain of Chromosome 16q" @default.
- NCIT_C175955 subClassOf B1c625d5b9e354911285fc706770d8293 @default.
- NCIT_C175955 subClassOf B6a0398f627907f43240bc7962840669f @default.
- NCIT_C175955 subClassOf NCIT_C175955 @default.
- NCIT_C175955 subClassOf NCIT_C2950 @default.
- NCIT_C175955 subClassOf NCIT_C36438 @default.
- NCIT_C175955 subClassOf NCIT_C3910 @default.
- NCIT_C175955 subClassOf NCIT_C6825 @default.