PubMed:15200408 JSONTXT 27 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
890 29-34 OrganismTaxon denotes human NCBITaxon:9606
891 35-44 GeneOrGeneProduct denotes uroplakin NCBIGene:11045|NCBIGene:7380
892 54-75 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux MESH:C564042
893 137-158 DiseaseOrPhenotypicFeature denotes vesicoureteral reflux MESH:C564042
894 160-163 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
895 170-189 DiseaseOrPhenotypicFeature denotes hereditary disorder MESH:D030342
896 343-362 DiseaseOrPhenotypicFeature denotes hereditary diseases MESH:D030342
897 379-390 DiseaseOrPhenotypicFeature denotes nephropathy MESH:D007674
898 416-439 DiseaseOrPhenotypicFeature denotes end-stage renal failure MESH:D007676
899 513-518 OrganismTaxon denotes mouse NCBITaxon:10090
900 519-537 GeneOrGeneProduct denotes uroplakin (UP) III NCBIGene:22270
901 647-650 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
902 655-669 DiseaseOrPhenotypicFeature denotes hydronephrosis MESH:D006869
903 723-725 GeneOrGeneProduct denotes UP NCBIGene:11045|NCBIGene:7380
904 753-758 OrganismTaxon denotes human NCBITaxon:9606
905 759-762 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
906 786-788 GeneOrGeneProduct denotes UP NCBIGene:11045|NCBIGene:7380
907 801-809 OrganismTaxon denotes patients NCBITaxon:9606
908 845-848 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
909 1162-1165 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
910 1214-1217 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
911 1298-1301 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
912 1302-1310 OrganismTaxon denotes patients NCBITaxon:9606
913 1425-1428 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
914 1447-1452 GeneOrGeneProduct denotes UP Ia NCBIGene:11045
915 1470-1476 SequenceVariant denotes C to T DBSNP:rs373513519
916 1495-1502 SequenceVariant denotes Ala7Val DBSNP:rs373513519
917 1523-1529 GeneOrGeneProduct denotes UP III NCBIGene:7380
918 1542-1548 SequenceVariant denotes C to G c|SUB|C||G
919 1566-1575 SequenceVariant denotes Pro154Ala p|SUB|P|154|A
920 1616-1619 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
921 1766-1772 GeneOrGeneProduct denotes UP III NCBIGene:7380
922 1781-1784 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
923 1982-1991 GeneOrGeneProduct denotes uroplakin NCBIGene:11045|NCBIGene:7380
924 2037-2040 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
925 2044-2050 OrganismTaxon denotes humans NCBITaxon:9606
926 2219-2222 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
927 2223-2231 OrganismTaxon denotes patients NCBITaxon:9606
928 2293-2299 GeneOrGeneProduct denotes UP III NCBIGene:22270
929 2309-2313 OrganismTaxon denotes mice NCBITaxon:10090
930 2347-2350 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042
931 2368-2382 DiseaseOrPhenotypicFeature denotes hydronephrosis MESH:D006869
932 2387-2401 DiseaseOrPhenotypicFeature denotes neonatal death MESH:D066087
933 2437-2446 GeneOrGeneProduct denotes uroplakin NCBIGene:11045|NCBIGene:7380
934 2505-2511 OrganismTaxon denotes humans NCBITaxon:9606