Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C172356> ?p ?o ?g. }
Showing items 1 to 31 of
31
with 100 items per page.
- NCIT_C172356 IAO_0000115 "A mutation in the TSC1 gene that is associated with an increased risk of disease." @default.
- NCIT_C172356 NCIT_NHC0 "C172356" @default.
- NCIT_C172356 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C172356 NCIT_P107 "Deleterious TSC1 Gene Mutation" @default.
- NCIT_C172356 NCIT_P108 "Deleterious TSC1 Gene Mutation" @default.
- NCIT_C172356 NCIT_P208 "CL1406487" @default.
- NCIT_C172356 NCIT_P322 "CTRP" @default.
- NCIT_C172356 NCIT_R177 NCIT_C16612 @default.
- NCIT_C172356 NCIT_R177 NCIT_C18259 @default.
- NCIT_C172356 NCIT_R177 NCIT_C21295 @default.
- NCIT_C172356 normalizedInformationContent "100" @default.
- NCIT_C172356 referenceCount "1" @default.
- NCIT_C172356 hasExactSynonym "Deleterious Hamartin Gene Mutation" @default.
- NCIT_C172356 hasExactSynonym "Deleterious TSC Gene Mutation" @default.
- NCIT_C172356 hasExactSynonym "Deleterious TSC1 Gene Mutation" @default.
- NCIT_C172356 hasExactSynonym "Deleterious TSC1 Mutation" @default.
- NCIT_C172356 hasExactSynonym "Deleterious Tuberous Sclerosis 1 Gene Mutation" @default.
- NCIT_C172356 inSubset NCIT_C116977 @default.
- NCIT_C172356 inSubset NCIT_C142799 @default.
- NCIT_C172356 inSubset NCIT_C142800 @default.
- NCIT_C172356 type Class @default.
- NCIT_C172356 isDefinedBy ncit.owl @default.
- NCIT_C172356 label "Deleterious TSC1 Gene Mutation" @default.
- NCIT_C172356 subClassOf NCIT_C118398 @default.
- NCIT_C172356 subClassOf NCIT_C172356 @default.
- NCIT_C172356 subClassOf NCIT_C36391 @default.
- NCIT_C172356 subClassOf NCIT_C3910 @default.
- NCIT_C172356 subClassOf NCIT_C45576 @default.
- NCIT_C172356 subClassOf NCIT_C93102 @default.
- NCIT_C172356 subClassOf NCIT_C97926 @default.
- NCIT_C172356 subClassOf NCIT_C97927 @default.