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- NCIT_C175328 IAO_0000115 "A change in the nucleotide sequence of the KMT2C gene that inhibits expression or results in the translation of either low-activity or inactive forms of the histone-lysine N- methyltransferase 2C protein." @default.
- NCIT_C175328 NCIT_NHC0 "C175328" @default.
- NCIT_C175328 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C175328 NCIT_P107 "Inactivating KMT2C Gene Mutation" @default.
- NCIT_C175328 NCIT_P108 "Inactivating KMT2C Gene Mutation" @default.
- NCIT_C175328 NCIT_P208 "CL1412627" @default.
- NCIT_C175328 NCIT_P322 "CTRP" @default.
- NCIT_C175328 NCIT_R177 NCIT_C16612 @default.
- NCIT_C175328 NCIT_R177 NCIT_C21281 @default.
- NCIT_C175328 NCIT_R177 NCIT_C25870 @default.
- NCIT_C175328 NCIT_R177 NCIT_C26110 @default.
- NCIT_C175328 NCIT_R177 NCIT_C93091 @default.
- NCIT_C175328 normalizedInformationContent "100" @default.
- NCIT_C175328 referenceCount "1" @default.
- NCIT_C175328 hasExactSynonym "Inactivating HALR Gene Mutation" @default.
- NCIT_C175328 hasExactSynonym "Inactivating KMT2C Gene Mutation" @default.
- NCIT_C175328 hasExactSynonym "Inactivating KMT2C Mutation" @default.
- NCIT_C175328 hasExactSynonym "Inactivating Lysine (K)-Specific Methyltransferase 2C Gene Mutation" @default.
- NCIT_C175328 hasExactSynonym "Inactivating Lysine Methyltransferase 2C Gene Mutation" @default.
- NCIT_C175328 hasExactSynonym "Inactivating MLL3 Gene Mutation" @default.
- NCIT_C175328 hasExactSynonym "Inactivating Myeloid/Lymphoid or Mixed-Lineage Leukemia 3 Gene Mutation" @default.
- NCIT_C175328 hasExactSynonym "KMT2C Gene Inactivation" @default.
- NCIT_C175328 hasExactSynonym "KMT2C Inactivating Gene Mutation" @default.
- NCIT_C175328 hasExactSynonym "KMT2C Inactivating Mutation" @default.
- NCIT_C175328 hasExactSynonym "KMT2C Inactivation" @default.
- NCIT_C175328 hasExactSynonym "KMT2C Loss of Function Gene Mutation" @default.
- NCIT_C175328 hasExactSynonym "KMT2C Loss of Function Mutation" @default.
- NCIT_C175328 hasExactSynonym "Loss of Function KMT2C Gene Mutation" @default.
- NCIT_C175328 hasExactSynonym "Loss of Function KMT2C Mutation" @default.
- NCIT_C175328 inSubset NCIT_C116977 @default.
- NCIT_C175328 inSubset NCIT_C142799 @default.
- NCIT_C175328 inSubset NCIT_C142800 @default.
- NCIT_C175328 type Class @default.
- NCIT_C175328 isDefinedBy ncit.owl @default.
- NCIT_C175328 label "Inactivating KMT2C Gene Mutation" @default.
- NCIT_C175328 subClassOf NCIT_C153252 @default.
- NCIT_C175328 subClassOf NCIT_C175328 @default.
- NCIT_C175328 subClassOf NCIT_C178119 @default.
- NCIT_C175328 subClassOf NCIT_C36327 @default.
- NCIT_C175328 subClassOf NCIT_C36391 @default.
- NCIT_C175328 subClassOf NCIT_C3910 @default.
- NCIT_C175328 subClassOf NCIT_C97926 @default.
- NCIT_C175328 subClassOf NCIT_C97927 @default.