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- NCIT_C189252 IAO_0000115 "A change in the nucleotide sequence of the TSC1 gene that originates in non-germline cells." @default.
- NCIT_C189252 NCIT_NHC0 "C189252" @default.
- NCIT_C189252 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C189252 NCIT_P108 "Somatic TSC1 Gene Mutation" @default.
- NCIT_C189252 NCIT_P208 "CL1794131" @default.
- NCIT_C189252 NCIT_R177 NCIT_C16612 @default.
- NCIT_C189252 NCIT_R177 NCIT_C18259 @default.
- NCIT_C189252 NCIT_R177 NCIT_C21295 @default.
- NCIT_C189252 normalizedInformationContent "92.730304365937428" @default.
- NCIT_C189252 referenceCount "3" @default.
- NCIT_C189252 hasExactSynonym "Somatic Hamartin Gene Mutation" @default.
- NCIT_C189252 hasExactSynonym "Somatic TSC Gene Mutation" @default.
- NCIT_C189252 hasExactSynonym "Somatic TSC1 Gene Mutation" @default.
- NCIT_C189252 hasExactSynonym "Somatic TSC1 Mutation" @default.
- NCIT_C189252 hasExactSynonym "Somatic Tuberous Sclerosis 1 Gene Mutation" @default.
- NCIT_C189252 type Class @default.
- NCIT_C189252 isDefinedBy ncit.owl @default.
- NCIT_C189252 label "Somatic TSC1 Gene Mutation" @default.
- NCIT_C189252 subClassOf NCIT_C118398 @default.
- NCIT_C189252 subClassOf NCIT_C18060 @default.
- NCIT_C189252 subClassOf NCIT_C189252 @default.
- NCIT_C189252 subClassOf NCIT_C36391 @default.
- NCIT_C189252 subClassOf NCIT_C3910 @default.
- NCIT_C189252 subClassOf NCIT_C45576 @default.
- NCIT_C189252 subClassOf NCIT_C97926 @default.
- NCIT_C189252 subClassOf NCIT_C97927 @default.