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PubMed:1493786 JSONTXT

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LitCoin-PubTator-for-Tuning

Id Subject Object Predicate Lexical cue tao:has_database_id
4 7-11 ChemicalEntity denotes urea MESH:D014508
5 16-23 ChemicalEntity denotes ammonia MESH:D000641
6 27-36 DiseaseOrPhenotypicFeature denotes epileptic MESH:D004827
7 37-45 OrganismTaxon denotes patients Tax:9606
25 88-92 ChemicalEntity denotes urea MESH:D014508
26 97-104 ChemicalEntity denotes ammonia MESH:D000641
27 122-130 OrganismTaxon denotes patients Tax:9606
28 156-164 DiseaseOrPhenotypicFeature denotes epilepsy MESH:D004827
29 166-174 OrganismTaxon denotes patients Tax:9606
30 188-196 DiseaseOrPhenotypicFeature denotes epilepsy MESH:D004827
31 300-304 ChemicalEntity denotes urea MESH:D014508
32 323-331 OrganismTaxon denotes patients Tax:9606
33 388-397 DiseaseOrPhenotypicFeature denotes epileptic MESH:D004827
34 419-426 ChemicalEntity denotes ammonia MESH:D000641
35 486-494 OrganismTaxon denotes patients Tax:9606
36 531-539 DiseaseOrPhenotypicFeature denotes epilepsy MESH:D004827
37 540-548 OrganismTaxon denotes patients Tax:9606
38 609-613 ChemicalEntity denotes urea MESH:D014508
39 618-625 ChemicalEntity denotes ammonia MESH:D000641
40 734-738 ChemicalEntity denotes urea MESH:D014508
41 862-872 DiseaseOrPhenotypicFeature denotes epilepsies MESH:D004827

LitCoin-Disease-Tuning-1

Id Subject Object Predicate Lexical cue ID:
T1 27-36 DiseaseOrPhenotypicFeature denotes epileptic DISEASE
T2 144-164 DiseaseOrPhenotypicFeature denotes generalized epilepsy D004829
T3 180-196 DiseaseOrPhenotypicFeature denotes partial epilepsy D004828
T4 388-397 DiseaseOrPhenotypicFeature denotes epileptic DISEASE
T5 519-539 DiseaseOrPhenotypicFeature denotes generalized epilepsy D004829
T6 854-872 DiseaseOrPhenotypicFeature denotes partial epilepsies D004828

LitEisuke

Id Subject Object Predicate Lexical cue #label
T1 27-36 DiseaseOrPhenotypicFeature denotes epileptic DISEASE
T2 144-164 DiseaseOrPhenotypicFeature denotes generalized epilepsy D004829
T3 180-196 DiseaseOrPhenotypicFeature denotes partial epilepsy D004828
T4 388-397 DiseaseOrPhenotypicFeature denotes epileptic DISEASE
T5 519-539 DiseaseOrPhenotypicFeature denotes generalized epilepsy D004829
T6 854-872 DiseaseOrPhenotypicFeature denotes partial epilepsies D004828

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 714-730 HP_0001939 denotes metabolic defect