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- NCIT_C45643 IAO_0000115 "A point mutation involving the substitution of Thymidine (a pyrimidine base) for Cytosine (a pyrimidine base) in a DNA sequence from eukaryotic or prokaryotic organisms. This abnormality can be either heritable or occur somatically." @default.
- NCIT_C45643 NCIT_NHC0 "C45643" @default.
- NCIT_C45643 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C45643 NCIT_P108 "Cytosine to Thymidine Transition Abnormality" @default.
- NCIT_C45643 NCIT_P207 "C1707606" @default.
- NCIT_C45643 NCIT_P366 "Cytosine_To_Thymidine_Transition_Abnormality" @default.
- NCIT_C45643 normalizedInformationContent "82.536929774922015" @default.
- NCIT_C45643 referenceCount "14" @default.
- NCIT_C45643 hasExactSynonym "Cytosine to Thymidine Mutation" @default.
- NCIT_C45643 hasExactSynonym "Cytosine to Thymidine Transition Abnormality" @default.
- NCIT_C45643 hasExactSynonym "Cytosine to Thymidine Transition" @default.
- NCIT_C45643 type Class @default.
- NCIT_C45643 isDefinedBy ncit.owl @default.
- NCIT_C45643 label "Cytosine to Thymidine Transition Abnormality" @default.
- NCIT_C45643 subClassOf NCIT_C18134 @default.
- NCIT_C45643 subClassOf NCIT_C36391 @default.
- NCIT_C45643 subClassOf NCIT_C3910 @default.
- NCIT_C45643 subClassOf NCIT_C45576 @default.
- NCIT_C45643 subClassOf NCIT_C45643 @default.
- NCIT_C45643 subClassOf NCIT_C62200 @default.
- NCIT_C45643 subClassOf NCIT_C97926 @default.