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- NCIT_C45648 IAO_0000115 "A point mutation involving the substitution of Adenosine (a purine 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_C45648 NCIT_NHC0 "C45648" @default.
- NCIT_C45648 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C45648 NCIT_P108 "Thymidine to Adenosine Transversion Abnormality" @default.
- NCIT_C45648 NCIT_P207 "C1710404" @default.
- NCIT_C45648 NCIT_P366 "Thymidine_To_Adenosine_Transversion_Abnormality" @default.
- NCIT_C45648 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C45648 referenceCount "2" @default.
- NCIT_C45648 hasExactSynonym "Thymidine to Adenosine Mutation" @default.
- NCIT_C45648 hasExactSynonym "Thymidine to Adenosine Transversion Abnormality" @default.
- NCIT_C45648 hasExactSynonym "Thymidine to Adenosine Transversion" @default.
- NCIT_C45648 type Class @default.
- NCIT_C45648 isDefinedBy ncit.owl @default.
- NCIT_C45648 label "Thymidine to Adenosine Transversion Abnormality" @default.
- NCIT_C45648 subClassOf NCIT_C18135 @default.
- NCIT_C45648 subClassOf NCIT_C36391 @default.
- NCIT_C45648 subClassOf NCIT_C3910 @default.
- NCIT_C45648 subClassOf NCIT_C45576 @default.
- NCIT_C45648 subClassOf NCIT_C45648 @default.
- NCIT_C45648 subClassOf NCIT_C62200 @default.
- NCIT_C45648 subClassOf NCIT_C97926 @default.