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- NCIT_C36632 IAO_0000115 "A cytogenetic abnormality that refers to loss of all or part of chromosome 19." @default.
- NCIT_C36632 NCIT_NHC0 "C36632" @default.
- NCIT_C36632 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C36632 NCIT_P108 "Loss of Chromosome 19" @default.
- NCIT_C36632 NCIT_P207 "C1517970" @default.
- NCIT_C36632 NCIT_P366 "Loss_of_Chromosome_19" @default.
- NCIT_C36632 NCIT_R173 NCIT_C12219 @default.
- NCIT_C36632 NCIT_R173 NCIT_C13202 @default.
- NCIT_C36632 NCIT_R173 NCIT_C13203 @default.
- NCIT_C36632 NCIT_R173 NCIT_C13214 @default.
- NCIT_C36632 NCIT_R173 NCIT_C13404 @default.
- NCIT_C36632 NCIT_R173 NCIT_C14134 @default.
- NCIT_C36632 NCIT_R173 NCIT_C21599 @default.
- NCIT_C36632 normalizedInformationContent "76.863042570845906" @default.
- NCIT_C36632 referenceCount "33" @default.
- NCIT_C36632 hasExactSynonym "Loss of Chromosome 19" @default.
- NCIT_C36632 hasExactSynonym "del(19)" @default.
- NCIT_C36632 type Class @default.
- NCIT_C36632 isDefinedBy ncit.owl @default.
- NCIT_C36632 label "Loss of Chromosome 19" @default.
- NCIT_C36632 subClassOf B7d8bf137a413929be96bea3d3a241f88 @default.
- NCIT_C36632 subClassOf Be5e6ffc41c17474e1acd82bc90dfcfa4 @default.
- NCIT_C36632 subClassOf NCIT_C2950 @default.
- NCIT_C36632 subClassOf NCIT_C36315 @default.
- NCIT_C36632 subClassOf NCIT_C36632 @default.
- NCIT_C36632 subClassOf NCIT_C3910 @default.
- NCIT_C36632 subClassOf NCIT_C6825 @default.