Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C131021> ?p ?o ?g. }
Showing items 1 to 31 of
31
with 100 items per page.
- NCIT_C131021 IAO_0000115 "A change in the nucleotide sequence of the TSHR gene." @default.
- NCIT_C131021 NCIT_NHC0 "C131021" @default.
- NCIT_C131021 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C131021 NCIT_P108 "TSHR Gene Mutation" @default.
- NCIT_C131021 NCIT_P208 "CL513363" @default.
- NCIT_C131021 NCIT_P322 "NICHD" @default.
- NCIT_C131021 NCIT_P325 "Mutation(s) in the TSHR gene, resulting in altered function of the thyroid stimulating hormone receptor." @default.
- NCIT_C131021 NCIT_R177 NCIT_C16612 @default.
- NCIT_C131021 NCIT_R177 NCIT_C20103 @default.
- NCIT_C131021 NCIT_R177 NCIT_C20923 @default.
- NCIT_C131021 NCIT_R177 NCIT_C21295 @default.
- NCIT_C131021 NCIT_R177 NCIT_C24881 @default.
- NCIT_C131021 normalizedInformationContent "90.826665450122817" @default.
- NCIT_C131021 referenceCount "4" @default.
- NCIT_C131021 hasExactSynonym "TSH Receptor Defect" @default.
- NCIT_C131021 hasExactSynonym "TSHR Gene Mutation" @default.
- NCIT_C131021 hasExactSynonym "Thyroid Simulating Hormone Receptor Gene Mutation" @default.
- NCIT_C131021 hasExactSynonym "Thyroid Stimulating Hormone Receptor Gene Mutation" @default.
- NCIT_C131021 hasExactSynonym "Thyrotropin Receptor Defect" @default.
- NCIT_C131021 inSubset NCIT_C118467 @default.
- NCIT_C131021 inSubset NCIT_C90259 @default.
- NCIT_C131021 type Class @default.
- NCIT_C131021 isDefinedBy ncit.owl @default.
- NCIT_C131021 label "TSHR Gene Mutation" @default.
- NCIT_C131021 subClassOf B48ebac90d2cf6ad1570654bc1de65a4b @default.
- NCIT_C131021 subClassOf B88420efe8ba20411a6a332a9616e0ebf @default.
- NCIT_C131021 subClassOf NCIT_C131021 @default.
- NCIT_C131021 subClassOf NCIT_C36391 @default.
- NCIT_C131021 subClassOf NCIT_C3910 @default.
- NCIT_C131021 subClassOf NCIT_C97926 @default.
- NCIT_C131021 subClassOf NCIT_C97927 @default.