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- NCIT_C199586 IAO_0000115 "A cytogenetic abnormality that refers to any inversion of genomic material on the X chromosome." @default.
- NCIT_C199586 NCIT_NHC0 "C199586" @default.
- NCIT_C199586 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C199586 NCIT_P108 "Chromosome X Inversion" @default.
- NCIT_C199586 NCIT_R173 NCIT_C12219 @default.
- NCIT_C199586 NCIT_R173 NCIT_C13202 @default.
- NCIT_C199586 NCIT_R173 NCIT_C13203 @default.
- NCIT_C199586 NCIT_R173 NCIT_C13285 @default.
- NCIT_C199586 NCIT_R173 NCIT_C13404 @default.
- NCIT_C199586 NCIT_R173 NCIT_C14134 @default.
- NCIT_C199586 NCIT_R173 NCIT_C21599 @default.
- NCIT_C199586 normalizedInformationContent "89.350088392419622" @default.
- NCIT_C199586 referenceCount "5" @default.
- NCIT_C199586 hasExactSynonym "Chromosome X Inversion" @default.
- NCIT_C199586 hasExactSynonym "Inversion of Chromosome X" @default.
- NCIT_C199586 hasExactSynonym "Inversion of X Chromosome" @default.
- NCIT_C199586 hasExactSynonym "X Chromosome Inversion" @default.
- NCIT_C199586 hasExactSynonym "inv(X)" @default.
- NCIT_C199586 type Class @default.
- NCIT_C199586 isDefinedBy ncit.owl @default.
- NCIT_C199586 label "Chromosome X Inversion" @default.
- NCIT_C199586 subClassOf B68f896a5f1bc6f41ead4bca51a6f8b17 @default.
- NCIT_C199586 subClassOf Bbd1fac9be957ad27e7e2b09955994c2b @default.
- NCIT_C199586 subClassOf NCIT_C199586 @default.
- NCIT_C199586 subClassOf NCIT_C2950 @default.
- NCIT_C199586 subClassOf NCIT_C36541 @default.
- NCIT_C199586 subClassOf NCIT_C3910 @default.
- NCIT_C199586 subClassOf NCIT_C6827 @default.