PubMed:16277682 JSONTXT 44 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
2466 17-22 SequenceVariant denotes M404V DBSNP:rs771966860
2467 39-42 GeneOrGeneProduct denotes p62 NCBIGene:8878
2468 43-57 GeneOrGeneProduct denotes sequestosome 1 NCBIGene:8878
2469 59-62 GeneOrGeneProduct denotes p62 NCBIGene:8878
2470 63-69 GeneOrGeneProduct denotes SQSTM1 NCBIGene:8878
2471 93-116 DiseaseOrPhenotypicFeature denotes Paget's disease of bone MESH:C538098
2472 156-159 GeneOrGeneProduct denotes p62 NCBIGene:8878
2473 160-174 GeneOrGeneProduct denotes Sequestosome 1 NCBIGene:8878
2474 181-184 GeneOrGeneProduct denotes p62 NCBIGene:8878
2475 185-191 GeneOrGeneProduct denotes SQSTM1 NCBIGene:8878
2476 241-264 DiseaseOrPhenotypicFeature denotes Paget's disease of bone MESH:C538098
2477 266-269 DiseaseOrPhenotypicFeature denotes PDB MESH:C538098
2478 298-343 SequenceVariant denotes methionine-->valine substitution at codon 404 DBSNP:rs771966860
2479 345-350 SequenceVariant denotes M404V DBSNP:rs771966860
2480 406-409 GeneOrGeneProduct denotes p62 NCBIGene:8878
2481 410-416 GeneOrGeneProduct denotes SQSTM1 NCBIGene:8878
2482 436-439 DiseaseOrPhenotypicFeature denotes PDB MESH:C538098
2483 440-447 OrganismTaxon denotes patient NCBITaxon:9606
2484 481-488 OrganismTaxon denotes patient NCBITaxon:9606
2485 541-544 DiseaseOrPhenotypicFeature denotes PDB MESH:C538098
2486 646-651 SequenceVariant denotes M404V DBSNP:rs771966860
2487 682-685 DiseaseOrPhenotypicFeature denotes PDB MESH:C538098
2488 854-857 DiseaseOrPhenotypicFeature denotes PDB MESH:C538098
2489 858-866 OrganismTaxon denotes patients NCBITaxon:9606
2490 991-996 SequenceVariant denotes M404V DBSNP:rs771966860
2491 1044-1047 DiseaseOrPhenotypicFeature denotes PDB MESH:C538098
2492 1060-1067 OrganismTaxon denotes patient NCBITaxon:9606
2493 1134-1153 DiseaseOrPhenotypicFeature denotes polyostotic disease MESH:D005357
2494 1317-1322 SequenceVariant denotes M404V DBSNP:rs771966860
2495 1411-1431 ChemicalEntity denotes alkaline phosphatase MESH:D000469
2496 1572-1577 SequenceVariant denotes M404V DBSNP:rs771966860
2497 1594-1597 GeneOrGeneProduct denotes p62 NCBIGene:8878
2498 1598-1604 GeneOrGeneProduct denotes SQSTM1 NCBIGene:8878
2499 1636-1639 DiseaseOrPhenotypicFeature denotes PDB MESH:C538098
2500 1683-1686 DiseaseOrPhenotypicFeature denotes PDB MESH:C538098
2501 1899-1902 GeneOrGeneProduct denotes p62 NCBIGene:8878
2502 1903-1909 GeneOrGeneProduct denotes SQSTM1 NCBIGene:8878
2503 1963-1966 DiseaseOrPhenotypicFeature denotes PDB MESH:C538098