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- NCIT_C175583 IAO_0000115 "A cytogenetic abnormality that involves a translocation between chromosomes 8 and 16." @default.
- NCIT_C175583 NCIT_A24 NCIT_C168895 @default.
- NCIT_C175583 NCIT_A24 NCIT_C3910 @default.
- NCIT_C175583 NCIT_NHC0 "C175583" @default.
- NCIT_C175583 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C175583 NCIT_P108 "t(8;16)" @default.
- NCIT_C175583 NCIT_P208 "CL1412944" @default.
- NCIT_C175583 NCIT_P322 "PCDC" @default.
- NCIT_C175583 NCIT_R173 NCIT_C12219 @default.
- NCIT_C175583 NCIT_R173 NCIT_C13202 @default.
- NCIT_C175583 NCIT_R173 NCIT_C13203 @default.
- NCIT_C175583 NCIT_R173 NCIT_C13211 @default.
- NCIT_C175583 NCIT_R173 NCIT_C13224 @default.
- NCIT_C175583 NCIT_R173 NCIT_C13404 @default.
- NCIT_C175583 NCIT_R173 NCIT_C14134 @default.
- NCIT_C175583 NCIT_R173 NCIT_C21599 @default.
- NCIT_C175583 normalizedInformationContent "100" @default.
- NCIT_C175583 referenceCount "1" @default.
- NCIT_C175583 hasExactSynonym "t(8;16)" @default.
- NCIT_C175583 inSubset NCIT_C173233 @default.
- NCIT_C175583 inSubset NCIT_C173236 @default.
- NCIT_C175583 inSubset NCIT_C174019 @default.
- NCIT_C175583 type Class @default.
- NCIT_C175583 isDefinedBy ncit.owl @default.
- NCIT_C175583 label "t(8;16)" @default.
- NCIT_C175583 subClassOf B0b18590a321a373201c1d67bfbde9314 @default.
- NCIT_C175583 subClassOf B167907eadeed48c26ae368f600173170 @default.
- NCIT_C175583 subClassOf B4d51565622f6fe71bf83b958b8f85cc4 @default.
- NCIT_C175583 subClassOf B966624962d3a3d140123316cacc76885 @default.
- NCIT_C175583 subClassOf NCIT_C175583 @default.
- NCIT_C175583 subClassOf NCIT_C2950 @default.
- NCIT_C175583 subClassOf NCIT_C3420 @default.
- NCIT_C175583 subClassOf NCIT_C36541 @default.
- NCIT_C175583 subClassOf NCIT_C3910 @default.