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LitCoin-entities-OrganismTaxon-PD

Id Subject Object Predicate Lexical cue db_id
T1 505-509 OrganismTaxon denotes rats NCBItxid:10118|NCBItxid:10116|NCBItxid:10114
T4 756-760 OrganismTaxon denotes rats NCBItxid:10118|NCBItxid:10116|NCBItxid:10114
T7 810-814 OrganismTaxon denotes rats NCBItxid:10118|NCBItxid:10116|NCBItxid:10114
T10 911-915 OrganismTaxon denotes rats NCBItxid:10118|NCBItxid:10116|NCBItxid:10114
T13 987-991 OrganismTaxon denotes rats NCBItxid:10118|NCBItxid:10116|NCBItxid:10114
T16 1099-1103 OrganismTaxon denotes rats NCBItxid:10118|NCBItxid:10116|NCBItxid:10114
T19 1207-1210 OrganismTaxon denotes rat NCBItxid:10116|NCBItxid:10114
T21 1371-1377 OrganismTaxon denotes humans NCBItxid:9605

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-88 Sentence denotes Pilocarpine seizures cause age-dependent impairment in auditory location discrimination.
T2 89-255 Sentence denotes Children who have status epilepticus have continuous or rapidly repeating seizures that may be life-threatening and may cause life-long changes in brain and behavior.
T3 256-349 Sentence denotes The extent to which status epilepticus causes deficits in auditory discrimination is unknown.
T4 350-484 Sentence denotes A naturalistic auditory location discrimination method was used to evaluate this question using an animal model of status epilepticus.
T5 485-611 Sentence denotes Male Sprague-Dawley rats were injected with saline on postnatal day (P) 20, or a convulsant dose of pilocarpine on P20 or P45.
T6 612-802 Sentence denotes Pilocarpine on either day induced status epilepticus; status epilepticus at P45 resulted in CA3 cell loss and spontaneous seizures, whereas P20 rats had no cell loss or spontaneous seizures.
T7 803-889 Sentence denotes Mature rats were trained with sound-source location and sound-silence discriminations.
T8 890-958 Sentence denotes Control (saline P20) rats acquired both discriminations immediately.
T9 959-1073 Sentence denotes In status epilepticus (P20) rats, acquisition of the sound-source location discrimination was moderately impaired.
T10 1074-1184 Sentence denotes Status epilepticus (P45) rats failed to acquire either sound-source location or sound-silence discriminations.
T11 1185-1284 Sentence denotes Status epilepticus in rat causes an age-dependent, long-term impairment in auditory discrimination.
T12 1285-1378 Sentence denotes This impairment may explain one cause of impaired auditory location discrimination in humans.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
2927 0-11 ChemicalEntity denotes Pilocarpine MESH:D010862
2928 12-20 DiseaseOrPhenotypicFeature denotes seizures MESH:D012640
2929 41-87 DiseaseOrPhenotypicFeature denotes impairment in auditory location discrimination MESH:D001308
2930 107-125 DiseaseOrPhenotypicFeature denotes status epilepticus MESH:D013226
2931 163-171 DiseaseOrPhenotypicFeature denotes seizures MESH:D012640
2932 276-294 DiseaseOrPhenotypicFeature denotes status epilepticus MESH:D013226
2933 302-337 DiseaseOrPhenotypicFeature denotes deficits in auditory discrimination MESH:D001308
2934 465-483 DiseaseOrPhenotypicFeature denotes status epilepticus MESH:D013226
2935 505-509 OrganismTaxon denotes rats NCBITaxon:10116
2936 585-596 ChemicalEntity denotes pilocarpine MESH:D010862
2937 612-623 ChemicalEntity denotes Pilocarpine MESH:D010862
2938 646-664 DiseaseOrPhenotypicFeature denotes status epilepticus MESH:D013226
2939 666-684 DiseaseOrPhenotypicFeature denotes status epilepticus MESH:D013226
2940 704-707 CellLine denotes CA3 NCBITaxon:10090
2941 734-742 DiseaseOrPhenotypicFeature denotes seizures MESH:D012640
2942 756-760 OrganismTaxon denotes rats NCBITaxon:10116
2943 793-801 DiseaseOrPhenotypicFeature denotes seizures MESH:D012640
2944 810-814 OrganismTaxon denotes rats NCBITaxon:10116
2945 911-915 OrganismTaxon denotes rats NCBITaxon:10116
2946 962-980 DiseaseOrPhenotypicFeature denotes status epilepticus MESH:D013226
2947 987-991 OrganismTaxon denotes rats NCBITaxon:10116
2948 1074-1092 DiseaseOrPhenotypicFeature denotes Status epilepticus MESH:D013226
2949 1099-1103 OrganismTaxon denotes rats NCBITaxon:10116
2950 1185-1203 DiseaseOrPhenotypicFeature denotes Status epilepticus MESH:D013226
2951 1207-1210 OrganismTaxon denotes rat NCBITaxon:10116
2952 1246-1283 DiseaseOrPhenotypicFeature denotes impairment in auditory discrimination MESH:D001308
2953 1326-1367 DiseaseOrPhenotypicFeature denotes impaired auditory location discrimination MESH:D001308
2954 1371-1377 OrganismTaxon denotes humans NCBITaxon:9606

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 107-125 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T2 276-294 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T3 465-483 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T4 646-664 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T5 666-684 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T6 916-924 DiseaseOrPhenotypicFeature denotes acquired 0021141
T7 962-980 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T8 1074-1092 DiseaseOrPhenotypicFeature denotes Status epilepticus 0002125
T9 1114-1121 DiseaseOrPhenotypicFeature denotes acquire 0021141
T10 1185-1203 DiseaseOrPhenotypicFeature denotes Status epilepticus 0002125

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 12-20 GeneOrGeneProduct denotes seizures
T2 163-171 GeneOrGeneProduct denotes seizures
T3 236-241 GeneOrGeneProduct denotes brain
T4 246-254 GeneOrGeneProduct denotes behavior
T5 341-348 GeneOrGeneProduct denotes unknown
T6 398-404 GeneOrGeneProduct denotes method
T7 704-707 GeneOrGeneProduct denotes CA3
T8 708-712 GeneOrGeneProduct denotes cell
T9 722-742 GeneOrGeneProduct denotes spontaneous seizures
T10 768-772 GeneOrGeneProduct denotes cell
T11 781-801 GeneOrGeneProduct denotes spontaneous seizures
T12 1241-1245 GeneOrGeneProduct denotes term

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 12-20 GeneOrGeneProduct denotes seizures
T2 163-171 GeneOrGeneProduct denotes seizures
T3 220-224 GeneOrGeneProduct denotes long
T4 236-241 GeneOrGeneProduct denotes brain
T5 246-254 GeneOrGeneProduct denotes behavior
T6 341-348 GeneOrGeneProduct denotes unknown
T7 398-404 GeneOrGeneProduct denotes method
T8 485-489 GeneOrGeneProduct denotes Male
T9 557-563 GeneOrGeneProduct denotes 20, or
T10 638-645 GeneOrGeneProduct denotes induced
T11 704-707 GeneOrGeneProduct denotes CA3
T12 708-712 GeneOrGeneProduct denotes cell
T13 722-742 GeneOrGeneProduct denotes spontaneous seizures
T14 768-772 GeneOrGeneProduct denotes cell
T15 781-801 GeneOrGeneProduct denotes spontaneous seizures
T16 803-809 GeneOrGeneProduct denotes Mature
T17 833-838 GeneOrGeneProduct denotes sound
T18 859-864 GeneOrGeneProduct denotes sound
T19 1012-1017 GeneOrGeneProduct denotes sound
T20 1129-1134 GeneOrGeneProduct denotes sound
T21 1154-1159 GeneOrGeneProduct denotes sound
T22 1236-1240 GeneOrGeneProduct denotes long
T23 1241-1245 GeneOrGeneProduct denotes term

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 12-20 DiseaseOrPhenotypicFeature denotes seizures D012640
T2 107-125 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T3 163-171 DiseaseOrPhenotypicFeature denotes seizures D012640
T4 276-294 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T5 465-483 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T6 646-664 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T7 666-684 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T8 734-742 DiseaseOrPhenotypicFeature denotes seizures D012640
T9 793-801 DiseaseOrPhenotypicFeature denotes seizures D012640
T10 962-980 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T11 1074-1092 DiseaseOrPhenotypicFeature denotes Status epilepticus D013226
T12 1185-1203 DiseaseOrPhenotypicFeature denotes Status epilepticus D013226

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 704-707 GeneOrGeneProduct denotes CA3
T2 722-742 GeneOrGeneProduct denotes spontaneous seizures
T3 781-801 GeneOrGeneProduct denotes spontaneous seizures

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 107-125 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T2 276-294 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T3 465-483 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T4 646-664 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T5 666-684 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T6 962-980 DiseaseOrPhenotypicFeature denotes status epilepticus 0002125
T7 1074-1092 DiseaseOrPhenotypicFeature denotes Status epilepticus 0002125
T8 1185-1203 DiseaseOrPhenotypicFeature denotes Status epilepticus 0002125

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 12-20 DiseaseOrPhenotypicFeature denotes seizures D012640
T2 41-87 DiseaseOrPhenotypicFeature denotes impairment in auditory location discrimination DISEASE
T3 107-125 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T4 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
T8 646-664 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T9 666-684 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T10 734-742 DiseaseOrPhenotypicFeature denotes seizures D012640
T11 793-801 DiseaseOrPhenotypicFeature denotes seizures D012640
T12 962-980 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T13 1074-1092 DiseaseOrPhenotypicFeature denotes Status epilepticus D013226
T14 1185-1203 DiseaseOrPhenotypicFeature denotes Status epilepticus D013226
T15 1246-1283 DiseaseOrPhenotypicFeature denotes impairment in auditory discrimination DISEASE
T16 1326-1367 DiseaseOrPhenotypicFeature denotes impaired auditory location discrimination DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 12-20 DiseaseOrPhenotypicFeature denotes seizures D012640
T2 41-87 DiseaseOrPhenotypicFeature denotes impairment in auditory location discrimination DISEASE
T3 107-125 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T4 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
T8 646-664 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T9 666-684 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T10 734-742 DiseaseOrPhenotypicFeature denotes seizures D012640
T11 793-801 DiseaseOrPhenotypicFeature denotes seizures D012640
T12 962-980 DiseaseOrPhenotypicFeature denotes status epilepticus D013226
T13 1074-1092 DiseaseOrPhenotypicFeature denotes Status epilepticus D013226
T14 1185-1203 DiseaseOrPhenotypicFeature denotes Status epilepticus D013226
T15 1246-1283 DiseaseOrPhenotypicFeature denotes impairment in auditory discrimination DISEASE
T16 1326-1367 DiseaseOrPhenotypicFeature denotes impaired auditory location discrimination DISEASE

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 0-11 ChemicalEntity denotes Pilocarpine http://purl.obolibrary.org/obo/CHEBI_8207
T2 585-596 ChemicalEntity denotes pilocarpine D010862|http://purl.obolibrary.org/obo/CHEBI_39462
T4 612-623 ChemicalEntity denotes Pilocarpine http://purl.obolibrary.org/obo/CHEBI_8207

LitCoin-NCBITaxon-2

Id Subject Object Predicate Lexical cue
T1 505-509 OrganismTaxon denotes rats
T2 756-760 OrganismTaxon denotes rats
T3 810-814 OrganismTaxon denotes rats
T4 911-915 OrganismTaxon denotes rats
T5 987-991 OrganismTaxon denotes rats
T6 1099-1103 OrganismTaxon denotes rats
T7 1207-1210 OrganismTaxon denotes rat
T8 1371-1377 OrganismTaxon denotes humans

LitCoin-training-merged

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