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- NCIT_C165248 IAO_0000115 "A cytogenetic abnormality that involves a translocation between chromosomes 17 and 19." @default.
- NCIT_C165248 NCIT_NHC0 "C165248" @default.
- NCIT_C165248 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C165248 NCIT_P107 "t(17;19)" @default.
- NCIT_C165248 NCIT_P108 "t(17;19)" @default.
- NCIT_C165248 NCIT_P208 "CL978549" @default.
- NCIT_C165248 NCIT_P322 "CTRP" @default.
- NCIT_C165248 NCIT_R173 NCIT_C12219 @default.
- NCIT_C165248 NCIT_R173 NCIT_C13202 @default.
- NCIT_C165248 NCIT_R173 NCIT_C13203 @default.
- NCIT_C165248 NCIT_R173 NCIT_C13212 @default.
- NCIT_C165248 NCIT_R173 NCIT_C13214 @default.
- NCIT_C165248 NCIT_R173 NCIT_C13404 @default.
- NCIT_C165248 NCIT_R173 NCIT_C14134 @default.
- NCIT_C165248 NCIT_R173 NCIT_C21599 @default.
- NCIT_C165248 normalizedInformationContent "100" @default.
- NCIT_C165248 referenceCount "1" @default.
- NCIT_C165248 hasExactSynonym "t(17;19)" @default.
- NCIT_C165248 inSubset NCIT_C116977 @default.
- NCIT_C165248 inSubset NCIT_C142799 @default.
- NCIT_C165248 inSubset NCIT_C142800 @default.
- NCIT_C165248 type Class @default.
- NCIT_C165248 isDefinedBy ncit.owl @default.
- NCIT_C165248 label "t(17;19)" @default.
- NCIT_C165248 subClassOf B0d000c29e59c78253d5af8f9c1722942 @default.
- NCIT_C165248 subClassOf B189c3cb7bdaba0a48226612c348975b7 @default.
- NCIT_C165248 subClassOf NCIT_C129438 @default.
- NCIT_C165248 subClassOf NCIT_C165248 @default.
- NCIT_C165248 subClassOf NCIT_C2950 @default.
- NCIT_C165248 subClassOf NCIT_C3420 @default.
- NCIT_C165248 subClassOf NCIT_C36541 @default.
- NCIT_C165248 subClassOf NCIT_C3910 @default.