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- NCIT_C45650 IAO_0000115 "A point mutation involving the substitution of Adenosine (a purine 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_C45650 NCIT_NHC0 "C45650" @default.
- NCIT_C45650 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C45650 NCIT_P108 "Cytosine to Adenosine Transversion Abnormality" @default.
- NCIT_C45650 NCIT_P207 "C1707604" @default.
- NCIT_C45650 NCIT_P366 "Cytosine_To_Adenosine_Transversion_Abnormality" @default.
- NCIT_C45650 normalizedInformationContent "92.730304365937428" @default.
- NCIT_C45650 referenceCount "3" @default.
- NCIT_C45650 hasExactSynonym "Cytosine to Adenosine Mutation" @default.
- NCIT_C45650 hasExactSynonym "Cytosine to Adenosine Transversion Abnormality" @default.
- NCIT_C45650 hasExactSynonym "Cytosine to Adenosine Transversion" @default.
- NCIT_C45650 type Class @default.
- NCIT_C45650 isDefinedBy ncit.owl @default.
- NCIT_C45650 label "Cytosine to Adenosine Transversion Abnormality" @default.
- NCIT_C45650 subClassOf NCIT_C18135 @default.
- NCIT_C45650 subClassOf NCIT_C36391 @default.
- NCIT_C45650 subClassOf NCIT_C3910 @default.
- NCIT_C45650 subClassOf NCIT_C45576 @default.
- NCIT_C45650 subClassOf NCIT_C45650 @default.
- NCIT_C45650 subClassOf NCIT_C62200 @default.
- NCIT_C45650 subClassOf NCIT_C97926 @default.