PubMed:20534762 JSONTXT 33 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID:
T1 27-30 ChemicalEntity denotes TSH http://purl.obolibrary.org/obo/CHEBI_137741|http://purl.obolibrary.org/obo/CHEBI_17842
T89104 27-35 GeneOrGeneProduct denotes TSH-beta
T69120 71-93 DiseaseOrPhenotypicFeature denotes central hypothyroidism D007037
T3 119-122 ChemicalEntity denotes TSH http://purl.obolibrary.org/obo/CHEBI_137741|http://purl.obolibrary.org/obo/CHEBI_17842
T5 157-160 ChemicalEntity denotes TSH http://purl.obolibrary.org/obo/CHEBI_137741|http://purl.obolibrary.org/obo/CHEBI_17842
T2 157-165 GeneOrGeneProduct denotes TSH-beta
T3451 186-211 DiseaseOrPhenotypicFeature denotes congenital hypothyroidism D003409
T7 226-229 ChemicalEntity denotes TSH http://purl.obolibrary.org/obo/CHEBI_137741|http://purl.obolibrary.org/obo/CHEBI_17842
T9 395-398 ChemicalEntity denotes TSH http://purl.obolibrary.org/obo/CHEBI_137741|http://purl.obolibrary.org/obo/CHEBI_17842
T5945 395-403 GeneOrGeneProduct denotes TSH-beta
T90879 430-438 OrganismTaxon denotes patients
T62466 455-477 DiseaseOrPhenotypicFeature denotes central hypothyroidism D007037
T54252 515-521 DiseaseOrPhenotypicFeature denotes anemia D000740
T87381 532-539 OrganismTaxon denotes Patient
T4 843-859 GeneOrGeneProduct denotes putative product
T88293 978-985 OrganismTaxon denotes patient
T33335 1066-1073 SequenceVariant denotes 313delT
T76614 1209-1213 SequenceVariant denotes C88Y
T11 1227-1243 ChemicalEntity denotes cysteine residue http://purl.obolibrary.org/obo/CHEBI_32460
T48940 1289-1298 OrganismTaxon denotes placental
T8897 1299-1311 GeneOrGeneProduct denotes glycoprotein
T6 1320-1333 GeneOrGeneProduct denotes beta subunits
T21214 1383-1387 SequenceVariant denotes C88Y
T12790 1519-1523 SequenceVariant denotes C88Y
T12 1580-1583 ChemicalEntity denotes TSH http://purl.obolibrary.org/obo/CHEBI_137741|http://purl.obolibrary.org/obo/CHEBI_17842
T65195 1580-1594 DiseaseOrPhenotypicFeature denotes TSH deficiency D007037
T95573 1656-1685 DiseaseOrPhenotypicFeature denotes isolated pituitary deficiency DISEASE
T31863 1760-1782 DiseaseOrPhenotypicFeature denotes central hypothyroidism D007037
T8 1833-1839 DiseaseOrPhenotypicFeature denotes anemia D000740