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- NCIT_C96865 IAO_0000115 "A molecular genetic abnormality indicating the presence of mutations in the AKT family of genes. This family includes the AKT1, AKT2, and AKT3 genes that are located on chromosomes 14, 19, and 1, respectively." @default.
- NCIT_C96865 NCIT_A13 NCIT_C18350 @default.
- NCIT_C96865 NCIT_A13 NCIT_C18352 @default.
- NCIT_C96865 NCIT_A13 NCIT_C20937 @default.
- NCIT_C96865 NCIT_NHC0 "C96865" @default.
- NCIT_C96865 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C96865 NCIT_P107 "AKT Family Gene Mutation" @default.
- NCIT_C96865 NCIT_P108 "AKT Family Gene Mutation" @default.
- NCIT_C96865 NCIT_P207 "C3273086" @default.
- NCIT_C96865 NCIT_P322 "CTRP" @default.
- NCIT_C96865 normalizedInformationContent "76.105970727550996" @default.
- NCIT_C96865 referenceCount "37" @default.
- NCIT_C96865 hasExactSynonym "AKT Family Gene Mutation" @default.
- NCIT_C96865 hasExactSynonym "AKT Gene Mutation" @default.
- NCIT_C96865 hasExactSynonym "AKT Serine/Threonine Kinase Family Gene Mutation" @default.
- NCIT_C96865 hasExactSynonym "AKT mutation" @default.
- NCIT_C96865 hasExactSynonym "v-akt Murine Thymoma Viral Oncogene Homolog Gene Family Mutation" @default.
- NCIT_C96865 inSubset NCIT_C116977 @default.
- NCIT_C96865 inSubset NCIT_C142799 @default.
- NCIT_C96865 inSubset NCIT_C142800 @default.
- NCIT_C96865 type Class @default.
- NCIT_C96865 isDefinedBy ncit.owl @default.
- NCIT_C96865 label "AKT Family Gene Mutation" @default.
- NCIT_C96865 subClassOf NCIT_C36327 @default.
- NCIT_C96865 subClassOf NCIT_C36391 @default.
- NCIT_C96865 subClassOf NCIT_C3910 @default.
- NCIT_C96865 subClassOf NCIT_C96865 @default.
- NCIT_C96865 subClassOf NCIT_C97926 @default.