PubMed:19067809 JSONTXT 25 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
5592 105-110 GeneOrGeneProduct denotes renin NCBIGene:5972
5593 111-122 GeneOrGeneProduct denotes angiotensin NCBIGene:183
5594 127-136 ChemicalEntity denotes serotonin MESH:D012701
5595 195-200 GeneOrGeneProduct denotes renin NCBIGene:5972
5596 201-212 GeneOrGeneProduct denotes angiotensin NCBIGene:183
5597 224-245 GeneOrGeneProduct denotes serotonin transporter NCBIGene:6532
5598 366-374 OrganismTaxon denotes patients NCBITaxon:9606
5599 380-397 DiseaseOrPhenotypicFeature denotes vasovagal syncope MESH:D019462
5600 435-443 OrganismTaxon denotes patients NCBITaxon:9606
5601 472-475 OrganismTaxon denotes men NCBITaxon:9606
5602 481-486 OrganismTaxon denotes women NCBITaxon:9606
5603 554-583 GeneOrGeneProduct denotes angiotensin-converting enzyme NCBIGene:1636
5604 621-624 GeneOrGeneProduct denotes ACE NCBIGene:1636
5605 627-642 GeneOrGeneProduct denotes angiotensinogen NCBIGene:183
5606 662-667 SequenceVariant denotes M 235 p|Allele|M|235
5607 670-700 GeneOrGeneProduct denotes angiotensin II receptor type 1 NCBIGene:185
5608 702-706 GeneOrGeneProduct denotes ATR1 NCBIGene:185
5609 722-730 SequenceVariant denotes A 11666C DBSNP:rs5186
5610 753-774 GeneOrGeneProduct denotes serotonin transporter NCBIGene:6532
5611 781-788 GeneOrGeneProduct denotes 5HTTLPR NCBIGene:6532
5612 1023-1030 SequenceVariant denotes A 1166C DBSNP:rs5186
5613 1531-1538 DiseaseOrPhenotypicFeature denotes syncope MESH:D013575
5614 1636-1643 SequenceVariant denotes A 1166C DBSNP:rs5186
5615 1664-1668 GeneOrGeneProduct denotes ATR1 NCBIGene:185
5616 1697-1708 DiseaseOrPhenotypicFeature denotes hypotension MESH:D007022
5617 1791-1808 DiseaseOrPhenotypicFeature denotes vasovagal syncope MESH:D019462