PubMed:16288199 JSONTXT 25 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue db_id
2543 26-47 GeneOrGeneProduct denotes nitric oxide synthase NCBIGene:4843
2544 62-70 DiseaseOrPhenotypicFeature denotes glaucoma MESH:D005901
2545 134-146 ChemicalEntity denotes Nitric oxide MESH:D009569
2546 184-189 OrganismTaxon denotes human NCBITaxon:9606
2547 346-389 DiseaseOrPhenotypicFeature denotes neurological and non-neurological disorders MESH:D009422
2548 475-496 GeneOrGeneProduct denotes Nitric Oxide Synthase NCBIGene:4843
2549 498-502 GeneOrGeneProduct denotes iNOS NCBIGene:4843
2550 512-547 DiseaseOrPhenotypicFeature denotes neuropathological disorder glaucoma MESH:D005901
2551 576-585 DiseaseOrPhenotypicFeature denotes blindness MESH:D001766
2552 670-674 GeneOrGeneProduct denotes iNOS NCBIGene:4843
2553 679-706 DiseaseOrPhenotypicFeature denotes primary open angle glaucoma MESH:D005902
2554 708-712 DiseaseOrPhenotypicFeature denotes POAG MESH:D005902
2555 925-929 GeneOrGeneProduct denotes iNOS NCBIGene:4843
2556 952-956 DiseaseOrPhenotypicFeature denotes POAG MESH:D005902
2557 957-965 OrganismTaxon denotes patients NCBITaxon:9606
2558 1229-1237 OrganismTaxon denotes patients NCBITaxon:9606
2559 1252-1261 SequenceVariant denotes (CCTTT)14 c|DUP||CCTTT|14
2560 1373-1377 DiseaseOrPhenotypicFeature denotes POAG MESH:D005902
2561 1378-1386 OrganismTaxon denotes patients NCBITaxon:9606
2562 1394-1403 SequenceVariant denotes (CCTTT)10 c|DUP||CCTTT|10
2563 1408-1417 SequenceVariant denotes (CCTTT)13 c|DUP||CCTTT|13
2564 1449-1458 SequenceVariant denotes (CCTTT)14 c|DUP||CCTTT|14
2565 1669-1673 GeneOrGeneProduct denotes iNOS NCBIGene:4843
2566 1679-1683 DiseaseOrPhenotypicFeature denotes POAG MESH:D005902