PubMed:21903317 JSONTXT 51 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
8851 53-58 GeneOrGeneProduct denotes renin NCBIGene:5972
8852 77-83 DiseaseOrPhenotypicFeature denotes anemia MESH:D000740
8853 85-98 DiseaseOrPhenotypicFeature denotes hyperuricemia MESH:D033461
8854 104-107 DiseaseOrPhenotypicFeature denotes CKD MESH:D051436
8855 158-163 GeneOrGeneProduct denotes renin NCBIGene:5972
8856 165-168 GeneOrGeneProduct denotes REN NCBIGene:5972
8857 176-200 DiseaseOrPhenotypicFeature denotes renal tubular dysgenesis MESH:C537048
8858 228-233 DiseaseOrPhenotypicFeature denotes death MESH:D003643
8859 250-264 DiseaseOrPhenotypicFeature denotes kidney failure MESH:D051437
8860 269-289 DiseaseOrPhenotypicFeature denotes pulmonary hypoplasia MESH:D008171
8861 319-328 DiseaseOrPhenotypicFeature denotes fetopathy MESH:C576203
8862 339-378 ChemicalEntity denotes angiotensin-converting enzyme inhibitor MESH:D000806
8863 382-410 ChemicalEntity denotes angiotensin receptor blocker MESH:D057911
8864 459-462 GeneOrGeneProduct denotes REN NCBIGene:5972
8865 509-522 DiseaseOrPhenotypicFeature denotes hyperuricemia MESH:D033461
8866 524-530 DiseaseOrPhenotypicFeature denotes anemia MESH:D000740
8867 536-558 DiseaseOrPhenotypicFeature denotes chronic kidney disease MESH:D051436
8868 560-563 DiseaseOrPhenotypicFeature denotes CKD MESH:D051436
8869 605-608 GeneOrGeneProduct denotes REN NCBIGene:5972
8870 675-678 GeneOrGeneProduct denotes REN NCBIGene:5972
8871 704-717 DiseaseOrPhenotypicFeature denotes hyperuricemia MESH:D033461
8872 722-725 DiseaseOrPhenotypicFeature denotes CKD MESH:D051436
8873 778-782 GeneOrGeneProduct denotes UMOD NCBIGene:7369
8874 784-794 GeneOrGeneProduct denotes uromodulin NCBIGene:7369
8875 800-805 GeneOrGeneProduct denotes HNF1B NCBIGene:6928
8876 807-835 GeneOrGeneProduct denotes hepatocyte nuclear factor 1β NCBIGene:6928
8877 883-928 SequenceVariant denotes thymidine to cytosine mutation at position 28 c|SUB|T|28|C
8878 936-939 GeneOrGeneProduct denotes REN NCBIGene:5972
8879 978-1030 SequenceVariant denotes tryptophan to arginine substitution at amino acid 10 p|SUB|W|10|R
8880 1075-1082 SequenceVariant denotes c.28T>C c|SUB|T|28|C
8881 1084-1090 SequenceVariant denotes p.W10R p|SUB|W|10|R
8882 1125-1128 GeneOrGeneProduct denotes REN NCBIGene:5972
8883 1158-1166 OrganismTaxon denotes patients NCBITaxon:9606
8884 1172-1175 DiseaseOrPhenotypicFeature denotes CKD MESH:D051436
8885 1268-1271 GeneOrGeneProduct denotes REN NCBIGene:5972
8886 1319-1325 DiseaseOrPhenotypicFeature denotes anemia MESH:D000740
8887 1327-1340 DiseaseOrPhenotypicFeature denotes hyperuricemia MESH:D033461
8888 1346-1349 DiseaseOrPhenotypicFeature denotes CKD MESH:D051436
8889 1351-1357 DiseaseOrPhenotypicFeature denotes Anemia MESH:D000740
8890 1458-1461 GeneOrGeneProduct denotes REN NCBIGene:5972
8891 1552-1555 GeneOrGeneProduct denotes REN NCBIGene:5972
8892 1565-1573 OrganismTaxon denotes patients NCBITaxon:9606
8893 1579-1582 DiseaseOrPhenotypicFeature denotes CKD MESH:D051436
8894 1588-1601 DiseaseOrPhenotypicFeature denotes hyperuricemia MESH:D033461
8895 1606-1612 DiseaseOrPhenotypicFeature denotes anemia MESH:D000740