PubMed:17600377 JSONTXT 40 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue db_id
4203 18-38 ChemicalEntity denotes maltolyl p-coumarate MESH:C524754
4204 51-69 DiseaseOrPhenotypicFeature denotes cognitive deficits MESH:D003072
4205 125-133 DiseaseOrPhenotypicFeature denotes dementia MESH:D003704
4206 260-280 ChemicalEntity denotes maltolyl p-coumarate MESH:C524754
4207 306-312 ChemicalEntity denotes maltol MESH:C008316
4208 317-332 ChemicalEntity denotes p-coumaric acid MESH:C495469
4209 380-400 ChemicalEntity denotes maltolyl p-coumarate MESH:C524754
4210 415-432 DiseaseOrPhenotypicFeature denotes cognitive decline MESH:D003072
4211 436-447 ChemicalEntity denotes scopolamine MESH:D012601
4212 457-461 OrganismTaxon denotes rats NCBITaxon:10116
4213 469-495 ChemicalEntity denotes amyloid beta peptide(1-42) MESH:C544092
4214 504-508 OrganismTaxon denotes rats NCBITaxon:10116
4215 510-530 ChemicalEntity denotes Maltolyl p-coumarate MESH:C524754
4216 554-572 DiseaseOrPhenotypicFeature denotes cognitive deficits MESH:D003072
4217 581-584 OrganismTaxon denotes rat NCBITaxon:10116
4218 691-717 ChemicalEntity denotes amyloid beta peptide(1-42) MESH:C544092
4219 726-730 OrganismTaxon denotes rats NCBITaxon:10116
4220 780-800 ChemicalEntity denotes maltolyl p-coumarate MESH:C524754
4221 816-823 CellLine denotes SH-SY5Y NCBITaxon:9606
4222 858-878 ChemicalEntity denotes maltolyl p-coumarate MESH:C524754
4223 898-924 ChemicalEntity denotes amyloid beta peptide(1-42) MESH:C544092
4224 926-935 ChemicalEntity denotes glutamate MESH:D018698
4225 939-943 ChemicalEntity denotes H2O2 MESH:D006861
4226 959-979 ChemicalEntity denotes maltolyl p-coumarate MESH:C524754
4227 1037-1060 ChemicalEntity denotes reactive oxygen species MESH:D017382
4228 1062-1074 ChemicalEntity denotes cytochrome c MESH:D045304
4229 1088-1097 GeneOrGeneProduct denotes caspase 3 NCBIGene:25402
4230 1186-1206 ChemicalEntity denotes maltolyl p-coumarate MESH:C524754
4231 1252-1271 DiseaseOrPhenotypicFeature denotes Alzheimer's disease MESH:D000544
4232 1309-1323 DiseaseOrPhenotypicFeature denotes neuronal death MESH:D009410
4233 1340-1369 DiseaseOrPhenotypicFeature denotes decline of cognitive function MESH:D003072