PubMed:20523265 JSONTXT 32 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
7411 21-40 GeneOrGeneProduct denotes complement factor H NCBIGene:3075
7412 42-44 GeneOrGeneProduct denotes C2 NCBIGene:717
7413 46-49 GeneOrGeneProduct denotes CFB NCBIGene:629
7414 55-57 GeneOrGeneProduct denotes C3 NCBIGene:718
7415 62-94 DiseaseOrPhenotypicFeature denotes age-related macular degeneration MESH:D008268
7416 176-195 GeneOrGeneProduct denotes complement factor H NCBIGene:3075
7417 197-200 GeneOrGeneProduct denotes CFH NCBIGene:3075
7418 203-208 GeneOrGeneProduct denotes C2/BF NCBIGene:629|NCBIGene:717
7419 214-216 GeneOrGeneProduct denotes C3 NCBIGene:718
7420 259-291 DiseaseOrPhenotypicFeature denotes age-related macular degeneration MESH:D008268
7421 293-296 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268
7422 500-508 OrganismTaxon denotes patients NCBITaxon:9606
7423 518-521 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268
7424 526-534 OrganismTaxon denotes patients NCBITaxon:9606
7425 545-551 DiseaseOrPhenotypicFeature denotes drusen MESH:D005128
7426 652-655 GeneOrGeneProduct denotes CFH NCBIGene:3075
7427 672-674 GeneOrGeneProduct denotes C2 NCBIGene:717
7428 676-679 GeneOrGeneProduct denotes CFB NCBIGene:629
7429 686-688 GeneOrGeneProduct denotes C3 NCBIGene:718
7430 780-785 GeneOrGeneProduct denotes CFHR1 NCBIGene:3078
7431 790-795 GeneOrGeneProduct denotes CFHR3 NCBIGene:10878
7432 906-915 SequenceVariant denotes rs3753394 DBSNP:rs3753394
7433 930-938 SequenceVariant denotes rs800292 DBSNP:rs800292
7434 953-962 SequenceVariant denotes rs1061170 DBSNP:rs1061170
7435 982-991 SequenceVariant denotes rs1329428 DBSNP:rs1329428
7436 1009-1012 GeneOrGeneProduct denotes CFH NCBIGene:3075
7437 1055-1058 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268
7438 1176-1179 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268
7439 1298-1307 SequenceVariant denotes rs2274700 DBSNP:rs2274700
7440 1312-1321 SequenceVariant denotes rs1410996 DBSNP:rs1410996
7441 1366-1369 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268
7442 1431-1434 GeneOrGeneProduct denotes CFH NCBIGene:3075
7443 1473-1479 DiseaseOrPhenotypicFeature denotes drusen MESH:D005128
7444 1505-1508 GeneOrGeneProduct denotes CFH NCBIGene:3075
7445 1510-1512 GeneOrGeneProduct denotes C2 NCBIGene:717
7446 1514-1517 GeneOrGeneProduct denotes CFB NCBIGene:629
7447 1523-1525 GeneOrGeneProduct denotes C3 NCBIGene:718
7448 1575-1578 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268
7449 1582-1588 DiseaseOrPhenotypicFeature denotes drusen MESH:D005128
7450 1622-1627 GeneOrGeneProduct denotes CFHR1 NCBIGene:3078
7451 1632-1637 GeneOrGeneProduct denotes CFHR3 NCBIGene:10878
7452 1725-1728 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268
7453 1732-1738 DiseaseOrPhenotypicFeature denotes drusen MESH:D005128
7454 1780-1789 SequenceVariant denotes rs3753394 DBSNP:rs3753394
7455 1804-1812 SequenceVariant denotes rs800292 DBSNP:rs800292
7456 1827-1836 SequenceVariant denotes rs1061170 DBSNP:rs1061170
7457 1856-1865 SequenceVariant denotes rs1329428 DBSNP:rs1329428
7458 1888-1897 SequenceVariant denotes rs7535263 DBSNP:rs7535263
7459 1899-1908 SequenceVariant denotes rs1410996 DBSNP:rs1410996
7460 1913-1922 SequenceVariant denotes rs2274700 DBSNP:rs2274700
7461 1927-1930 GeneOrGeneProduct denotes CFH NCBIGene:3075
7462 1970-1973 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268
7463 2035-2038 GeneOrGeneProduct denotes CFH NCBIGene:3075
7464 2061-2064 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268
7465 2127-2132 GeneOrGeneProduct denotes CFHR1 NCBIGene:3078
7466 2137-2142 GeneOrGeneProduct denotes CFHR3 NCBIGene:10878
7467 2262-2265 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268
7468 2291-2293 GeneOrGeneProduct denotes C2 NCBIGene:717
7469 2295-2298 GeneOrGeneProduct denotes CFB NCBIGene:629
7470 2304-2306 GeneOrGeneProduct denotes C3 NCBIGene:718
7471 2351-2354 DiseaseOrPhenotypicFeature denotes AMD MESH:D008268