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- NCIT_C93106 IAO_0000115 "A gene mutation in an individual that was not present in or transmitted from their ancestors. This type of mutation generally occurs spontaneously during the process of cell division-associated DNA replication during embryonic or fetal development." @default.
- NCIT_C93106 NCIT_NHC0 "C93106" @default.
- NCIT_C93106 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C93106 NCIT_P107 "de novo Mutation" @default.
- NCIT_C93106 NCIT_P108 "de novo Mutation" @default.
- NCIT_C93106 NCIT_P207 "C2985439" @default.
- NCIT_C93106 NCIT_P322 "CTRP" @default.
- NCIT_C93106 NCIT_P325 "An alteration in a gene that is present for the first time in one family member as a result of a mutation in a germ cell (egg or sperm) of one of the parents, or a mutation that arises in the fertilized egg itself during early embryogenesis." @default.
- NCIT_C93106 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C93106 referenceCount "2" @default.
- NCIT_C93106 hasExactSynonym "de novo Mutation" @default.
- NCIT_C93106 hasExactSynonym "de novo mutation" @default.
- NCIT_C93106 hasExactSynonym "new mutation" @default.
- NCIT_C93106 inSubset NCIT_C116977 @default.
- NCIT_C93106 inSubset NCIT_C142799 @default.
- NCIT_C93106 inSubset NCIT_C142800 @default.
- NCIT_C93106 type Class @default.
- NCIT_C93106 isDefinedBy ncit.owl @default.
- NCIT_C93106 label "de novo Mutation" @default.
- NCIT_C93106 subClassOf NCIT_C36391 @default.
- NCIT_C93106 subClassOf NCIT_C3910 @default.
- NCIT_C93106 subClassOf NCIT_C45576 @default.
- NCIT_C93106 subClassOf NCIT_C93106 @default.
- NCIT_C93106 subClassOf NCIT_C97926 @default.