PubMed:18681856 JSONTXT 31 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
5436 31-61 DiseaseOrPhenotypicFeature denotes non-autoimmune hyperthyroidism MESH:C563786
5437 102-109 SequenceVariant denotes p.M453T DBSNP:rs121908864
5438 118-138 GeneOrGeneProduct denotes thyrotropin receptor NCBIGene:7253
5439 220-250 DiseaseOrPhenotypicFeature denotes non-autoimmune hyperthyroidism MESH:C563786
5440 252-255 DiseaseOrPhenotypicFeature denotes NAH MESH:C563786
5441 306-326 GeneOrGeneProduct denotes thyrotropin receptor NCBIGene:7253
5442 328-332 GeneOrGeneProduct denotes TSHR NCBIGene:7253
5443 340-348 OrganismTaxon denotes PATIENTS NCBITaxon:9606
5444 638-642 GeneOrGeneProduct denotes TSHR NCBIGene:7253
5445 756-762 SequenceVariant denotes T to C DBSNP:rs121908864
5446 792-796 GeneOrGeneProduct denotes TSHR NCBIGene:7253
5447 803-814 SequenceVariant denotes c.1358T-->C DBSNP:rs121908864
5448 849-897 SequenceVariant denotes methionine (ATG) by threonine (ACG) at codon 453 DBSNP:rs121908864
5449 899-906 SequenceVariant denotes p.M453T DBSNP:rs121908864
5450 1049-1064 DiseaseOrPhenotypicFeature denotes hyperthyroidism MESH:D006980
5451 1066-1082 DiseaseOrPhenotypicFeature denotes ventriculomegaly MESH:D006849
5452 1250-1266 DiseaseOrPhenotypicFeature denotes Ventriculomegaly MESH:D006849
5453 1404-1407 DiseaseOrPhenotypicFeature denotes NAH MESH:C563786
5454 1433-1437 GeneOrGeneProduct denotes TSHR NCBIGene:7253