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- NCIT_C36579 IAO_0000115 "A cytogenetic abnormality that refers to the loss of all or part of the short arm of chromosome 18 (18p)." @default.
- NCIT_C36579 NCIT_NHC0 "C36579" @default.
- NCIT_C36579 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C36579 NCIT_P108 "Loss of Chromosome 18p" @default.
- NCIT_C36579 NCIT_P207 "C1517968" @default.
- NCIT_C36579 NCIT_P366 "Loss_of_Chromosome_18p" @default.
- NCIT_C36579 NCIT_R173 NCIT_C12219 @default.
- NCIT_C36579 NCIT_R173 NCIT_C13202 @default.
- NCIT_C36579 NCIT_R173 NCIT_C13203 @default.
- NCIT_C36579 NCIT_R173 NCIT_C13213 @default.
- NCIT_C36579 NCIT_R173 NCIT_C13404 @default.
- NCIT_C36579 NCIT_R173 NCIT_C14134 @default.
- NCIT_C36579 NCIT_R173 NCIT_C21599 @default.
- NCIT_C36579 normalizedInformationContent "86.239998175184226" @default.
- NCIT_C36579 referenceCount "8" @default.
- NCIT_C36579 hasExactSynonym "Loss of Chromosome 18p" @default.
- NCIT_C36579 hasExactSynonym "del(18p)" @default.
- NCIT_C36579 type Class @default.
- NCIT_C36579 isDefinedBy ncit.owl @default.
- NCIT_C36579 label "Loss of Chromosome 18p" @default.
- NCIT_C36579 subClassOf B216e83c5c2a8976514fb47e7765c5de6 @default.
- NCIT_C36579 subClassOf B6b99e79043a2e734964895b09323250a @default.
- NCIT_C36579 subClassOf NCIT_C2950 @default.
- NCIT_C36579 subClassOf NCIT_C36315 @default.
- NCIT_C36579 subClassOf NCIT_C36579 @default.
- NCIT_C36579 subClassOf NCIT_C3910 @default.
- NCIT_C36579 subClassOf NCIT_C6825 @default.