PubMed:20708777 JSONTXT 31 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
7844 44-51 GeneOrGeneProduct denotes CYP11B2 NCBIGene:1585
7845 52-59 GeneOrGeneProduct denotes CYP11B1 NCBIGene:1584
7846 84-96 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7847 109-117 OrganismTaxon denotes patients NCBITaxon:9606
7848 123-153 DiseaseOrPhenotypicFeature denotes aldosterone-producing adenomas MESH:D000236
7849 167-179 DiseaseOrPhenotypicFeature denotes Hypertension MESH:D006973
7850 292-304 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7851 480-503 GeneOrGeneProduct denotes steroid synthesis genes NCBIGene:1584|NCBIGene:1585
7852 505-512 GeneOrGeneProduct denotes CYP11B2 NCBIGene:1585
7853 514-521 GeneOrGeneProduct denotes CYP11B1 NCBIGene:1584
7854 559-571 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7855 583-591 OrganismTaxon denotes patients NCBITaxon:9606
7856 621-651 DiseaseOrPhenotypicFeature denotes aldosterone-producing adenomas MESH:D000236
7857 653-656 DiseaseOrPhenotypicFeature denotes APA MESH:D000236
7858 681-689 OrganismTaxon denotes patients NCBITaxon:9606
7859 695-698 DiseaseOrPhenotypicFeature denotes APA MESH:D000236
7860 745-757 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7861 763-771 OrganismTaxon denotes patients NCBITaxon:9606
7862 791-800 SequenceVariant denotes rs1799998 DBSNP:rs1799998
7863 802-809 SequenceVariant denotes C-344 T DBSNP:rs1799998
7864 833-839 SequenceVariant denotes rs4539 DBSNP:rs4539
7865 841-847 SequenceVariant denotes A2718G DBSNP:rs4539
7866 856-863 GeneOrGeneProduct denotes CYP11B2 NCBIGene:1585
7867 868-874 SequenceVariant denotes rs6410 DBSNP:rs6410
7868 876-882 SequenceVariant denotes G22 5A DBSNP:rs6410
7869 885-891 SequenceVariant denotes rs6387 DBSNP:rs6387
7870 893-899 SequenceVariant denotes A2803G DBSNP:rs6387
7871 908-915 GeneOrGeneProduct denotes CYP11B1 NCBIGene:1584
7872 942-950 GeneOrGeneProduct denotes CYPB11B2 NCBIGene:1585
7873 951-958 GeneOrGeneProduct denotes CYP11B1 NCBIGene:1584
7874 1002-1014 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7875 1064-1071 GeneOrGeneProduct denotes CYP11B2 NCBIGene:1585
7876 1072-1079 GeneOrGeneProduct denotes CYP11B1 NCBIGene:1584
7877 1135-1147 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7878 1159-1167 OrganismTaxon denotes patients NCBITaxon:9606
7879 1198-1201 DiseaseOrPhenotypicFeature denotes APA MESH:D000236
7880 1232-1238 SequenceVariant denotes rs4539 DBSNP:rs4539
7881 1302-1314 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7882 1480-1492 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7883 1595-1607 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7884 1629-1641 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7885 1672-1684 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7886 1763-1769 SequenceVariant denotes rs4539 DBSNP:rs4539
7887 1847-1859 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7888 1872-1880 OrganismTaxon denotes patients NCBITaxon:9606
7889 1911-1914 DiseaseOrPhenotypicFeature denotes APA MESH:D000236
7890 1937-1947 GeneOrGeneProduct denotes CYP11B2/B1 NCBIGene:1584|NCBIGene:1585
7891 1997-2009 DiseaseOrPhenotypicFeature denotes hypertension MESH:D006973
7892 2013-2021 OrganismTaxon denotes patients NCBITaxon:9606
7893 2027-2030 DiseaseOrPhenotypicFeature denotes APA MESH:D000236