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- NCIT_C86948 IAO_0000115 "A form of chromosomal variation characterized by the presence of an extra X chromosome in each cell of a human female." @default.
- NCIT_C86948 NCIT_NHC0 "C86948" @default.
- NCIT_C86948 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C86948 NCIT_P108 "Trisomy X" @default.
- NCIT_C86948 NCIT_P208 "CL521323" @default.
- NCIT_C86948 NCIT_R173 NCIT_C12219 @default.
- NCIT_C86948 NCIT_R173 NCIT_C13202 @default.
- NCIT_C86948 NCIT_R173 NCIT_C13203 @default.
- NCIT_C86948 NCIT_R173 NCIT_C13285 @default.
- NCIT_C86948 NCIT_R173 NCIT_C13404 @default.
- NCIT_C86948 NCIT_R173 NCIT_C14134 @default.
- NCIT_C86948 NCIT_R173 NCIT_C21599 @default.
- NCIT_C86948 normalizedInformationContent "100" @default.
- NCIT_C86948 referenceCount "1" @default.
- NCIT_C86948 hasExactSynonym "Trisomy X" @default.
- NCIT_C86948 type Class @default.
- NCIT_C86948 isDefinedBy ncit.owl @default.
- NCIT_C86948 label "Trisomy X" @default.
- NCIT_C86948 subClassOf B0a19db0109bb48c46647c66c57ebed99 @default.
- NCIT_C86948 subClassOf Bda150169299c25bbaf4cd16532a83140 @default.
- NCIT_C86948 subClassOf NCIT_C2873 @default.
- NCIT_C86948 subClassOf NCIT_C2950 @default.
- NCIT_C86948 subClassOf NCIT_C3421 @default.
- NCIT_C86948 subClassOf NCIT_C36331 @default.
- NCIT_C86948 subClassOf NCIT_C3910 @default.
- NCIT_C86948 subClassOf NCIT_C6825 @default.
- NCIT_C86948 subClassOf NCIT_C86948 @default.