PubMed:20335448 JSONTXT 34 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
7169 42-47 OrganismTaxon denotes human NCBITaxon:9606
7170 48-71 GeneOrGeneProduct denotes glucocorticoid receptor NCBIGene:2908
7171 91-116 DiseaseOrPhenotypicFeature denotes glucocorticoid resistance MESH:C564221
7172 196-221 DiseaseOrPhenotypicFeature denotes glucocorticoid resistance MESH:C564221
7173 314-329 ChemicalEntity denotes glucocorticoids MESH:D005938
7174 358-381 GeneOrGeneProduct denotes glucocorticoid receptor NCBIGene:2908
7175 383-385 GeneOrGeneProduct denotes GR NCBIGene:2908
7176 471-488 ChemicalEntity denotes mineralocorticoid MESH:D008901
7177 504-512 ChemicalEntity denotes androgen MESH:D000728
7178 601-608 OrganismTaxon denotes PATIENT NCBITaxon:9606
7179 666-691 DiseaseOrPhenotypicFeature denotes glucocorticoid resistance MESH:C564221
7180 706-713 OrganismTaxon denotes patient NCBITaxon:9606
7181 748-755 DiseaseOrPhenotypicFeature denotes seizure MESH:D012640
7182 772-784 DiseaseOrPhenotypicFeature denotes hypoglycemia MESH:D007003
7183 789-800 DiseaseOrPhenotypicFeature denotes hypokalemia MESH:D007008
7184 815-827 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7185 832-850 DiseaseOrPhenotypicFeature denotes premature pubarche MESH:C567552
7186 860-873 ChemicalEntity denotes dexamethasone MESH:D003907
7187 941-948 OrganismTaxon denotes patient NCBITaxon:9606
7188 951-953 GeneOrGeneProduct denotes GR NCBIGene:2908
7189 988-1023 SequenceVariant denotes (G-->A) at nucleotide position 2141 c|SUB|G|2141|A
7190 1068-1116 SequenceVariant denotes arginine by glutamine at amino acid position 714 c|SUB|R|714|Q
7191 1159-1167 GeneOrGeneProduct denotes GR alpha NCBIGene:2908
7192 1417-1450 GeneOrGeneProduct denotes p160 nuclear receptor coactivator NCBIGene:8648
7193 1516-1553 SequenceVariant denotes arginine by glutamine at position 714 c|SUB|R|714|Q
7194 1740-1753 ChemicalEntity denotes Dexamethasone MESH:D003907
7195 1796-1814 DiseaseOrPhenotypicFeature denotes premature pubarche MESH:C567552
7196 1816-1828 DiseaseOrPhenotypicFeature denotes hypoglycemia MESH:D007003
7197 1830-1842 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7198 1848-1859 DiseaseOrPhenotypicFeature denotes hypokalemia MESH:D007008
7199 1888-1900 SequenceVariant denotes arginine 714 c|Allele|R|714
7200 1999-2007 GeneOrGeneProduct denotes GR alpha NCBIGene:2908