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- NCIT_C45642 IAO_0000115 "A point mutation involving the substitution of Cytosine (a pyrimidine base) for Thymidine (a pyrimidine base) in a DNA sequence from eukaryotic or prokaryotic organisms. This abnormality can be either heritable or occur somatically." @default.
- NCIT_C45642 NCIT_NHC0 "C45642" @default.
- NCIT_C45642 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C45642 NCIT_P108 "Thymidine to Cytosine Transition Abnormality" @default.
- NCIT_C45642 NCIT_P207 "C1710405" @default.
- NCIT_C45642 NCIT_P366 "Thymidine_To_Cytosine_Transition_Abnormality" @default.
- NCIT_C45642 normalizedInformationContent "89.350088392419622" @default.
- NCIT_C45642 referenceCount "5" @default.
- NCIT_C45642 hasExactSynonym "Thymidine to Cytosine Mutation" @default.
- NCIT_C45642 hasExactSynonym "Thymidine to Cytosine Transition Abnormality" @default.
- NCIT_C45642 hasExactSynonym "Thymidine to Cytosine Transition" @default.
- NCIT_C45642 type Class @default.
- NCIT_C45642 isDefinedBy ncit.owl @default.
- NCIT_C45642 label "Thymidine to Cytosine Transition Abnormality" @default.
- NCIT_C45642 subClassOf NCIT_C18134 @default.
- NCIT_C45642 subClassOf NCIT_C36391 @default.
- NCIT_C45642 subClassOf NCIT_C3910 @default.
- NCIT_C45642 subClassOf NCIT_C45576 @default.
- NCIT_C45642 subClassOf NCIT_C45642 @default.
- NCIT_C45642 subClassOf NCIT_C62200 @default.
- NCIT_C45642 subClassOf NCIT_C97926 @default.