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PubMed:22946725 JSONTXT

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LitCoin-PubTator-for-Tuning

Id Subject Object Predicate Lexical cue tao:has_database_id
2 15-29 DiseaseOrPhenotypicFeature denotes gene disorders MESH:D006527
3 34-42 DiseaseOrPhenotypicFeature denotes epilepsy MESH:D004827
16 44-52 DiseaseOrPhenotypicFeature denotes Epilepsy MESH:D004827
17 175-188 DiseaseOrPhenotypicFeature denotes skin disorder MESH:D012871
18 224-234 DiseaseOrPhenotypicFeature denotes epilepsies MESH:D004827
19 468-478 DiseaseOrPhenotypicFeature denotes epilepsies MESH:D004827
20 502-516 DiseaseOrPhenotypicFeature denotes gene disorders MESH:D006527
21 595-621 DiseaseOrPhenotypicFeature denotes tuberous sclerosis complex MESH:D014402
22 623-631 DiseaseOrPhenotypicFeature denotes epilepsy MESH:D004827
23 648-661 DiseaseOrPhenotypicFeature denotes Rett syndrome MESH:D015518
24 687-707 DiseaseOrPhenotypicFeature denotes myoclonic epilepsies MESH:D004831
25 713-728 DiseaseOrPhenotypicFeature denotes novel disorders MESH:C000657245
26 737-745 DiseaseOrPhenotypicFeature denotes epilepsy MESH:D004827
27 779-786 GeneOrGeneProduct denotes PCDH 19 Gene:57526

LitCoin-Disease-Tuning-1

Id Subject Object Predicate Lexical cue ID:
T1 34-42 DiseaseOrPhenotypicFeature denotes epilepsy D004827
T2 44-52 DiseaseOrPhenotypicFeature denotes Epilepsy D004827
T3 147-170 DiseaseOrPhenotypicFeature denotes intellectual disability D008607
T4 224-234 DiseaseOrPhenotypicFeature denotes epilepsies D004827
T5 468-478 DiseaseOrPhenotypicFeature denotes epilepsies D004827
T6 577-586 DiseaseOrPhenotypicFeature denotes syndromes D013577
T7 595-621 DiseaseOrPhenotypicFeature denotes tuberous sclerosis complex D014402
T8 623-631 DiseaseOrPhenotypicFeature denotes epilepsy D004827
T9 648-661 DiseaseOrPhenotypicFeature denotes Rett syndrome D015518
T10 675-707 DiseaseOrPhenotypicFeature denotes progressive myoclonic epilepsies D020191
T11 737-745 DiseaseOrPhenotypicFeature denotes epilepsy D004827

LitEisuke

Id Subject Object Predicate Lexical cue #label
T1 34-42 DiseaseOrPhenotypicFeature denotes epilepsy D004827
T2 44-52 DiseaseOrPhenotypicFeature denotes Epilepsy D004827
T3 147-170 DiseaseOrPhenotypicFeature denotes intellectual disability D008607
T4 224-234 DiseaseOrPhenotypicFeature denotes epilepsies D004827
T5 468-478 DiseaseOrPhenotypicFeature denotes epilepsies D004827
T6 595-621 DiseaseOrPhenotypicFeature denotes tuberous sclerosis complex D014402
T7 623-631 DiseaseOrPhenotypicFeature denotes epilepsy D004827
T8 648-661 DiseaseOrPhenotypicFeature denotes Rett syndrome D015518
T9 675-707 DiseaseOrPhenotypicFeature denotes progressive myoclonic epilepsies D020191
T10 737-745 DiseaseOrPhenotypicFeature denotes epilepsy D004827

DisGeNET

Id Subject Object Predicate Lexical cue
T0 779-786 gene:57575 denotes PCDH 19
T1 675-707 disease:C0751778 denotes progressive myoclonic epilepsies
T2 779-786 gene:57526 denotes PCDH 19
T3 675-707 disease:C0751778 denotes progressive myoclonic epilepsies
T4 779-786 gene:57575 denotes PCDH 19
T5 737-745 disease:C0014544 denotes epilepsy
T6 779-786 gene:57526 denotes PCDH 19
T7 737-745 disease:C0014544 denotes epilepsy
R1 T0 T1 associated_with PCDH 19,progressive myoclonic epilepsies
R2 T2 T3 associated_with PCDH 19,progressive myoclonic epilepsies
R3 T4 T5 associated_with PCDH 19,epilepsy
R4 T6 T7 associated_with PCDH 19,epilepsy

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 147-170 HP_0001249 denotes intellectual disability
T2 175-188 HP_0000951 denotes skin disorder
T3 687-696 HP_0001336 denotes myoclonic

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
22946725-4#231#238#gene57575 779-786 gene57575 denotes PCDH 19
22946725-4#231#238#gene57526 779-786 gene57526 denotes PCDH 19
22946725-4#189#197#diseaseC0014544 737-745 diseaseC0014544 denotes epilepsy
231#238#gene57575189#197#diseaseC0014544 22946725-4#231#238#gene57575 22946725-4#189#197#diseaseC0014544 associated_with PCDH 19,epilepsy
231#238#gene57526189#197#diseaseC0014544 22946725-4#231#238#gene57526 22946725-4#189#197#diseaseC0014544 associated_with PCDH 19,epilepsy