PubMed:29049388 JSONTXT 23 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue #label ID:
T15197 13-18 OrganismTaxon denotes mouse
T12364 28-35 GeneOrGeneProduct denotes podocin
T24073 53-71 DiseaseOrPhenotypicFeature denotes nephrotic syndrome D009404
T2 90-95 GeneOrGeneProduct denotes NPHS2
T10911 111-118 GeneOrGeneProduct denotes podocin
T41330 137-155 DiseaseOrPhenotypicFeature denotes nephrotic syndrome D009404
T4 173-180 GeneOrGeneProduct denotes podocin
T66323 191-196 SequenceVariant denotes R138Q
T19913 262-285 DiseaseOrPhenotypicFeature denotes end-stage renal disease D007676
T57397 296-300 OrganismTaxon denotes mice
T35876 312-317 SequenceVariant denotes R140Q
T53346 332-337 OrganismTaxon denotes mouse
T89878 350-355 OrganismTaxon denotes human
T66714 356-361 SequenceVariant denotes R138Q
T70014 413-426 DiseaseOrPhenotypicFeature denotes renal failure D051437
T5 474-481 GeneOrGeneProduct denotes podocin
T6 503-508 GeneOrGeneProduct denotes NPHS2
T82040 509-514 SequenceVariant denotes R140Q
T1 526-535 ChemicalEntity denotes tamoxifen http://purl.obolibrary.org/obo/CHEBI_41774|D013629
T3 546-561 ChemicalEntity denotes Cre recombinase C045073
T80913 658-663 SequenceVariant denotes R140Q
T95215 709-720 DiseaseOrPhenotypicFeature denotes proteinuria D011507
T28747 799-812 DiseaseOrPhenotypicFeature denotes renal failure D051437
T63547 1250-1258 DiseaseOrPhenotypicFeature denotes fibrosis D005355
T53049 1346-1357 DiseaseOrPhenotypicFeature denotes proteinuria D011507
T82552 1389-1394 SequenceVariant denotes R140Q
T7 1395-1402 GeneOrGeneProduct denotes podocin
T8 1525-1532 GeneOrGeneProduct denotes miRNA21
T74446 1676-1681 SequenceVariant denotes R140Q
T9 1682-1689 GeneOrGeneProduct denotes podocin
T64328 1690-1695 OrganismTaxon denotes mouse
T40596 1761-1766 OrganismTaxon denotes human
T45427 1767-1785 DiseaseOrPhenotypicFeature denotes nephrotic syndrome D009404
T23115 1849-1854 OrganismTaxon denotes human
T10 2027-2038 DiseaseOrPhenotypicFeature denotes proteinuria D011507
T11 2040-2058 DiseaseOrPhenotypicFeature denotes glomerulosclerosis DISEASE
T12 2075-2088 DiseaseOrPhenotypicFeature denotes renal failure D051437