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- NCIT_C45645 IAO_0000115 "A point mutation involving the substitution of Cytosine (a pyrimidine base) for Adenosine (a purine base) in a DNA sequence from eukaryotic or prokaryotic organisms. This abnormality can be either heritable or occur somatically." @default.
- NCIT_C45645 NCIT_NHC0 "C45645" @default.
- NCIT_C45645 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C45645 NCIT_P108 "Adenosine to Cytosine Transversion Abnormality" @default.
- NCIT_C45645 NCIT_P207 "C1706716" @default.
- NCIT_C45645 NCIT_P366 "Adenosine_To_Cytosine_Transversion_Abnormality" @default.
- NCIT_C45645 normalizedInformationContent "89.350088392419622" @default.
- NCIT_C45645 referenceCount "5" @default.
- NCIT_C45645 hasExactSynonym "Adenosine to Cytosine Mutation" @default.
- NCIT_C45645 hasExactSynonym "Adenosine to Cytosine Transversion Abnormality" @default.
- NCIT_C45645 hasExactSynonym "Adenosine to Cytosine Transversion" @default.
- NCIT_C45645 type Class @default.
- NCIT_C45645 isDefinedBy ncit.owl @default.
- NCIT_C45645 label "Adenosine to Cytosine Transversion Abnormality" @default.
- NCIT_C45645 subClassOf NCIT_C18135 @default.
- NCIT_C45645 subClassOf NCIT_C36391 @default.
- NCIT_C45645 subClassOf NCIT_C3910 @default.
- NCIT_C45645 subClassOf NCIT_C45576 @default.
- NCIT_C45645 subClassOf NCIT_C45645 @default.
- NCIT_C45645 subClassOf NCIT_C62200 @default.
- NCIT_C45645 subClassOf NCIT_C97926 @default.