PubMed:15191352 JSONTXT 28 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
833 15-41 DiseaseOrPhenotypicFeature denotes thyroid hormone resistance MESH:D018382
834 47-54 OrganismTaxon denotes patient NCBITaxon:9606
835 94-105 GeneOrGeneProduct denotes T3 receptor NCBIGene:7068
836 112-150 DiseaseOrPhenotypicFeature denotes Resistance to thyroid hormone syndrome MESH:D018382
837 152-155 DiseaseOrPhenotypicFeature denotes RTH MESH:D018382
838 227-235 OrganismTaxon denotes Patients NCBITaxon:9606
839 241-244 DiseaseOrPhenotypicFeature denotes RTH MESH:D018382
840 323-337 DiseaseOrPhenotypicFeature denotes thyrotoxicosis MESH:D013971
841 353-367 DiseaseOrPhenotypicFeature denotes hypothyroidism MESH:D007037
842 436-465 GeneOrGeneProduct denotes thyroid hormone receptor beta NCBIGene:7068
843 472-479 GeneOrGeneProduct denotes TR-beta NCBIGene:7068
844 495-502 OrganismTaxon denotes patient NCBITaxon:9606
845 508-511 DiseaseOrPhenotypicFeature denotes RTH MESH:D018382
846 563-570 GeneOrGeneProduct denotes TR-beta NCBIGene:7068
847 612-617 SequenceVariant denotes I280S p|SUB|I|280|S
848 619-628 SequenceVariant denotes 1123T-->G g|SUB|T|1123|G
849 738-743 SequenceVariant denotes I280S p|SUB|I|280|S
850 793-800 OrganismTaxon denotes patient NCBITaxon:9606
851 838-871 DiseaseOrPhenotypicFeature denotes impaired intellectual development MESH:D008607
852 873-885 DiseaseOrPhenotypicFeature denotes hyperkinetic MESH:D006948
853 897-908 DiseaseOrPhenotypicFeature denotes tachycardia MESH:D013610
854 910-939 DiseaseOrPhenotypicFeature denotes hearing and visual impairment MESH:D006311|MESH:D014786
855 995-1000 SequenceVariant denotes I280S p|SUB|I|280|S
856 1050-1057 GeneOrGeneProduct denotes TR-beta NCBIGene:7068