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- NCIT_C99752 IAO_0000115 "A mutation class that includes insertion mutations, deletion mutations and mutation events where both an insertion and a deletion has occurred." @default.
- NCIT_C99752 NCIT_NHC0 "C99752" @default.
- NCIT_C99752 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C99752 NCIT_P108 "Indel Mutation" @default.
- NCIT_C99752 NCIT_P207 "C1956002" @default.
- NCIT_C99752 NCIT_P322 "CTDC" @default.
- NCIT_C99752 NCIT_P322 "FDA" @default.
- NCIT_C99752 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C99752 referenceCount "2" @default.
- NCIT_C99752 hasExactSynonym "INDEL" @default.
- NCIT_C99752 hasExactSynonym "Indel Mutation" @default.
- NCIT_C99752 hasExactSynonym "Indel" @default.
- NCIT_C99752 hasExactSynonym "Insertion-Deletion" @default.
- NCIT_C99752 hasExactSynonym "indel variant" @default.
- NCIT_C99752 hasExactSynonym "indel_variant" @default.
- NCIT_C99752 inSubset NCIT_C173071 @default.
- NCIT_C99752 inSubset NCIT_C188686 @default.
- NCIT_C99752 inSubset NCIT_C188687 @default.
- NCIT_C99752 type Class @default.
- NCIT_C99752 isDefinedBy ncit.owl @default.
- NCIT_C99752 label "Indel Mutation" @default.
- NCIT_C99752 subClassOf NCIT_C36391 @default.
- NCIT_C99752 subClassOf NCIT_C3910 @default.
- NCIT_C99752 subClassOf NCIT_C45576 @default.
- NCIT_C99752 subClassOf NCIT_C97926 @default.
- NCIT_C99752 subClassOf NCIT_C99752 @default.