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- NCIT_C128642 IAO_0000115 "A cytogenetic abnormality that involves a translocation between chromosomes 11 and 22." @default.
- NCIT_C128642 NCIT_NHC0 "C128642" @default.
- NCIT_C128642 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C128642 NCIT_P107 "t(11;22)" @default.
- NCIT_C128642 NCIT_P108 "t(11;22)" @default.
- NCIT_C128642 NCIT_P208 "CL509580" @default.
- NCIT_C128642 NCIT_P322 "CTRP" @default.
- NCIT_C128642 NCIT_R173 NCIT_C12219 @default.
- NCIT_C128642 NCIT_R173 NCIT_C13202 @default.
- NCIT_C128642 NCIT_R173 NCIT_C13203 @default.
- NCIT_C128642 NCIT_R173 NCIT_C13206 @default.
- NCIT_C128642 NCIT_R173 NCIT_C13218 @default.
- NCIT_C128642 NCIT_R173 NCIT_C13404 @default.
- NCIT_C128642 NCIT_R173 NCIT_C14134 @default.
- NCIT_C128642 NCIT_R173 NCIT_C21599 @default.
- NCIT_C128642 normalizedInformationContent "100" @default.
- NCIT_C128642 referenceCount "1" @default.
- NCIT_C128642 hasExactSynonym "t(11;22)" @default.
- NCIT_C128642 inSubset NCIT_C116977 @default.
- NCIT_C128642 inSubset NCIT_C142799 @default.
- NCIT_C128642 inSubset NCIT_C142800 @default.
- NCIT_C128642 type Class @default.
- NCIT_C128642 isDefinedBy ncit.owl @default.
- NCIT_C128642 label "t(11;22)" @default.
- NCIT_C128642 subClassOf B905cbc1cb2b30b0367b83ddcc33863af @default.
- NCIT_C128642 subClassOf Bbb29a32713fec818b6afa2956c03f3ad @default.
- NCIT_C128642 subClassOf Bd1784048d1d5baed70f5dfe8b12ff522 @default.
- NCIT_C128642 subClassOf Beefe08f4d4fc1de6145ed4e097a061f5 @default.
- NCIT_C128642 subClassOf NCIT_C128642 @default.
- NCIT_C128642 subClassOf NCIT_C2950 @default.
- NCIT_C128642 subClassOf NCIT_C3420 @default.
- NCIT_C128642 subClassOf NCIT_C36541 @default.
- NCIT_C128642 subClassOf NCIT_C3910 @default.