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- NCIT_C63429 IAO_0000115 "Any mutation within an intron, including the sequences that comprise the intron boundary." @default.
- NCIT_C63429 NCIT_A32 NCIT_C97926 @default.
- NCIT_C63429 NCIT_NHC0 "C63429" @default.
- NCIT_C63429 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C63429 NCIT_P108 "Intronic Mutation" @default.
- NCIT_C63429 NCIT_P207 "C1881250" @default.
- NCIT_C63429 NCIT_P322 "GDC" @default.
- NCIT_C63429 NCIT_P366 "Intronic_Mutation" @default.
- NCIT_C63429 NCIT_P375 "Intron Variant" @default.
- NCIT_C63429 normalizedInformationContent "87.123597049860606" @default.
- NCIT_C63429 referenceCount "7" @default.
- NCIT_C63429 hasExactSynonym "Intron Mutation" @default.
- NCIT_C63429 hasExactSynonym "Intron Variant" @default.
- NCIT_C63429 hasExactSynonym "Intronic Mutation" @default.
- NCIT_C63429 inSubset NCIT_C157711 @default.
- NCIT_C63429 inSubset NCIT_C177537 @default.
- NCIT_C63429 type Class @default.
- NCIT_C63429 isDefinedBy ncit.owl @default.
- NCIT_C63429 label "Intronic Mutation" @default.
- NCIT_C63429 subClassOf NCIT_C18093 @default.
- NCIT_C63429 subClassOf NCIT_C36327 @default.
- NCIT_C63429 subClassOf NCIT_C36391 @default.
- NCIT_C63429 subClassOf NCIT_C3910 @default.
- NCIT_C63429 subClassOf NCIT_C45576 @default.
- NCIT_C63429 subClassOf NCIT_C63429 @default.
- NCIT_C63429 subClassOf NCIT_C97926 @default.