PubMed:16596970 JSONTXT 23 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function

Id Subject Object Predicate Lexical cue #label ID:
T1 0-11 ChemicalEntity denotes Pilocarpine http://purl.obolibrary.org/obo/CHEBI_8207
T29434 12-20 DiseaseOrPhenotypicFeature denotes seizures D012640
T71660 41-87 DiseaseOrPhenotypicFeature denotes impairment in auditory location discrimination DISEASE
T70735 107-125 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T25477 163-171 DiseaseOrPhenotypicFeature denotes seizures D012640
T5 276-294 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T6 302-337 DiseaseOrPhenotypicFeature denotes deficits in auditory discrimination DISEASE
T7 465-483 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T36849 505-509 OrganismTaxon denotes rats
T2 585-596 ChemicalEntity denotes pilocarpine http://purl.obolibrary.org/obo/CHEBI_39462|D010862
T4 612-623 ChemicalEntity denotes Pilocarpine http://purl.obolibrary.org/obo/CHEBI_8207
T8 646-664 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T9 666-684 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T54782 704-707 GeneOrGeneProduct denotes CA3
T86940 722-742 GeneOrGeneProduct denotes spontaneous seizures
T10 734-742 DiseaseOrPhenotypicFeature denotes seizures D012640
T46808 756-760 OrganismTaxon denotes rats
T3 781-801 GeneOrGeneProduct denotes spontaneous seizures
T11 793-801 DiseaseOrPhenotypicFeature denotes seizures D012640
T33463 810-814 OrganismTaxon denotes rats
T37006 911-915 OrganismTaxon denotes rats
T12 962-980 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T55999 987-991 OrganismTaxon denotes rats
T13 1074-1092 DiseaseOrPhenotypicFeature denotes Status epilepticus D013226
T44360 1099-1103 OrganismTaxon denotes rats
T14 1185-1203 DiseaseOrPhenotypicFeature denotes Status epilepticus D013226
T8310 1207-1210 OrganismTaxon denotes rat
T15 1246-1283 DiseaseOrPhenotypicFeature denotes impairment in auditory discrimination DISEASE
T16 1326-1367 DiseaseOrPhenotypicFeature denotes impaired auditory location discrimination DISEASE
T87228 1371-1377 OrganismTaxon denotes humans