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- NCIT_C114473 IAO_0000115 "A chromosomal abnormality in which a somatic cell has a single member of each pair of homologous chromosomes." @default.
- NCIT_C114473 NCIT_NHC0 "C114473" @default.
- NCIT_C114473 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C114473 NCIT_P108 "Haploidy" @default.
- NCIT_C114473 NCIT_P207 "C0018590" @default.
- NCIT_C114473 normalizedInformationContent "100" @default.
- NCIT_C114473 referenceCount "1" @default.
- NCIT_C114473 hasExactSynonym "Haploid" @default.
- NCIT_C114473 hasExactSynonym "Haploidy" @default.
- NCIT_C114473 type Class @default.
- NCIT_C114473 isDefinedBy ncit.owl @default.
- NCIT_C114473 label "Haploidy" @default.
- NCIT_C114473 subClassOf NCIT_C114473 @default.
- NCIT_C114473 subClassOf NCIT_C2950 @default.
- NCIT_C114473 subClassOf NCIT_C3910 @default.
- NCIT_C114473 subClassOf NCIT_C6825 @default.