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- NCIT_C199593 IAO_0000115 "A cytogenetic abnormality that refers to a chromosomal translocation that involves the short arm (within p22-31) of chromosome 1 and the long arm (within q24-25) of chromosome 10." @default.
- NCIT_C199593 NCIT_NHC0 "C199593" @default.
- NCIT_C199593 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C199593 NCIT_P108 "t(1;10)(p22-31;q24-25)" @default.
- NCIT_C199593 NCIT_R173 NCIT_C12219 @default.
- NCIT_C199593 NCIT_R173 NCIT_C13202 @default.
- NCIT_C199593 NCIT_R173 NCIT_C13203 @default.
- NCIT_C199593 NCIT_R173 NCIT_C13204 @default.
- NCIT_C199593 NCIT_R173 NCIT_C13205 @default.
- NCIT_C199593 NCIT_R173 NCIT_C13404 @default.
- NCIT_C199593 NCIT_R173 NCIT_C14134 @default.
- NCIT_C199593 NCIT_R173 NCIT_C21599 @default.
- NCIT_C199593 normalizedInformationContent "100" @default.
- NCIT_C199593 referenceCount "1" @default.
- NCIT_C199593 hasExactSynonym "t(1;10)(p22-31;q24-25)" @default.
- NCIT_C199593 type Class @default.
- NCIT_C199593 isDefinedBy ncit.owl @default.
- NCIT_C199593 label "t(1;10)(p22-31;q24-25)" @default.
- NCIT_C199593 subClassOf B7183aff657e9752e8a2b52dee5d948ec @default.
- NCIT_C199593 subClassOf Be6191b6bb06087084230054eebb07406 @default.
- NCIT_C199593 subClassOf NCIT_C199593 @default.
- NCIT_C199593 subClassOf NCIT_C2950 @default.
- NCIT_C199593 subClassOf NCIT_C3420 @default.
- NCIT_C199593 subClassOf NCIT_C36386 @default.
- NCIT_C199593 subClassOf NCIT_C36541 @default.
- NCIT_C199593 subClassOf NCIT_C3910 @default.