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PubMed:20195852 JSONTXT 10 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID:
T1 8-19 DiseaseOrPhenotypicFeature denotes nephropathy DISEASE
T2 192-203 DiseaseOrPhenotypicFeature denotes nephropathy DISEASE
T3 205-208 DiseaseOrPhenotypicFeature denotes CIN DISEASE
T21154 232-240 OrganismTaxon denotes patients
T85826 389-397 OrganismTaxon denotes patients
T4 481-484 DiseaseOrPhenotypicFeature denotes CIN DISEASE
T69084 523-532 ChemicalEntity denotes iopromide http://purl.obolibrary.org/obo/CHEBI_63578|C038192
T9187 537-544 ChemicalEntity denotes iohexol http://purl.obolibrary.org/obo/CHEBI_31709|D007472
T97870 555-563 OrganismTaxon denotes patients
T5 692-700 DiseaseOrPhenotypicFeature denotes cyanosis D003490
T11787 709-717 OrganismTaxon denotes patients
T84707 761-770 ChemicalEntity denotes iopromide http://purl.obolibrary.org/obo/CHEBI_63578|C038192
T53980 792-799 ChemicalEntity denotes iohexol http://purl.obolibrary.org/obo/CHEBI_31709|D007472
T93206 825-831 ChemicalEntity denotes sodium http://purl.obolibrary.org/obo/CHEBI_26708|D012964
T56465 838-847 ChemicalEntity denotes potassium http://purl.obolibrary.org/obo/CHEBI_26216|D011188
T3880 857-867 ChemicalEntity denotes creatinine http://purl.obolibrary.org/obo/CHEBI_16737|D003404
T51492 869-871 ChemicalEntity denotes Cr D003404
T85965 1022-1024 ChemicalEntity denotes Cr D003404
T6 1074-1087 DiseaseOrPhenotypicFeature denotes renal failure D051437
T7 1103-1118 DiseaseOrPhenotypicFeature denotes kidney, Failure D051437
T8 1178-1190 DiseaseOrPhenotypicFeature denotes renal damage DISEASE
T93100 1192-1197 GeneOrGeneProduct denotes RIFLE
T9 1228-1231 DiseaseOrPhenotypicFeature denotes CIN DISEASE
T10 1301-1304 DiseaseOrPhenotypicFeature denotes CIN DISEASE
T51707 1305-1313 OrganismTaxon denotes patients
T35510 1336-1344 OrganismTaxon denotes patients
T11 1389-1401 DiseaseOrPhenotypicFeature denotes renal injury EisukeAdded
T12 1457-1469 DiseaseOrPhenotypicFeature denotes renal injury EisukeAdded
T59095 1492-1500 OrganismTaxon denotes patients
T13 1506-1509 DiseaseOrPhenotypicFeature denotes CIN DISEASE
T14 1688-1691 DiseaseOrPhenotypicFeature denotes CIN DISEASE
T43495 1757-1765 OrganismTaxon denotes patients
T58186 1771-1777 GeneOrGeneProduct denotes CIN, 6
T16 1791-1816 DiseaseOrPhenotypicFeature denotes congenital heart diseases D006330
T9640 1895-1903 OrganismTaxon denotes patients
T17 1945-1948 DiseaseOrPhenotypicFeature denotes CIN DISEASE
T18 2076-2084 DiseaseOrPhenotypicFeature denotes cyanosis D003490
T19 2099-2102 DiseaseOrPhenotypicFeature denotes CIN DISEASE