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- NCIT_C180942 IAO_0000115 "A cytogenetic abnormality that refers to any structural irregularity in chromosome 9." @default.
- NCIT_C180942 NCIT_NHC0 "C180942" @default.
- NCIT_C180942 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C180942 NCIT_P107 "Chromosome 9 Abnormality" @default.
- NCIT_C180942 NCIT_P108 "Chromosome 9 Abnormality" @default.
- NCIT_C180942 NCIT_P208 "CL1663623" @default.
- NCIT_C180942 NCIT_P322 "CTRP" @default.
- NCIT_C180942 NCIT_R173 NCIT_C12219 @default.
- NCIT_C180942 NCIT_R173 NCIT_C13202 @default.
- NCIT_C180942 NCIT_R173 NCIT_C13203 @default.
- NCIT_C180942 NCIT_R173 NCIT_C13225 @default.
- NCIT_C180942 NCIT_R173 NCIT_C13404 @default.
- NCIT_C180942 NCIT_R173 NCIT_C14134 @default.
- NCIT_C180942 NCIT_R173 NCIT_C21599 @default.
- NCIT_C180942 normalizedInformationContent "55.024315475172557" @default.
- NCIT_C180942 referenceCount "895" @default.
- NCIT_C180942 hasExactSynonym "Aberrant Chromosome 9" @default.
- NCIT_C180942 hasExactSynonym "Chromosome 9 Aberration" @default.
- NCIT_C180942 hasExactSynonym "Chromosome 9 Abnormality" @default.
- NCIT_C180942 inSubset NCIT_C116977 @default.
- NCIT_C180942 inSubset NCIT_C142799 @default.
- NCIT_C180942 inSubset NCIT_C142800 @default.
- NCIT_C180942 type Class @default.
- NCIT_C180942 isDefinedBy ncit.owl @default.
- NCIT_C180942 label "Chromosome 9 Abnormality" @default.
- NCIT_C180942 subClassOf B06a732c77860f903f51b02ce819b5b66 @default.
- NCIT_C180942 subClassOf B8fbb5e425269d3443a6e340ae4ce1da2 @default.
- NCIT_C180942 subClassOf NCIT_C180942 @default.
- NCIT_C180942 subClassOf NCIT_C2950 @default.
- NCIT_C180942 subClassOf NCIT_C3910 @default.