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PubMed:10353146 JSONTXT

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LitCoin-PubTator-for-Tuning

Id Subject Object Predicate Lexical cue tao:has_database_id
4 23-29 OrganismTaxon denotes infant Tax:9606
5 30-42 DiseaseOrPhenotypicFeature denotes sudden death MESH:D003645
6 51-78 DiseaseOrPhenotypicFeature denotes hypertrophic cardiomyopathy MESH:D002312
7 82-97 DiseaseOrPhenotypicFeature denotes Pompe's disease MESH:D006009
17 108-131 DiseaseOrPhenotypicFeature denotes storage disease type II MESH:D006009
18 133-148 DiseaseOrPhenotypicFeature denotes Pompe's disease MESH:D006009
19 160-188 DiseaseOrPhenotypicFeature denotes inherited metabolic disorder MESH:D008661
20 211-226 DiseaseOrPhenotypicFeature denotes infantile death MESH:D003643
21 239-253 DiseaseOrPhenotypicFeature denotes cardiomyopathy MESH:D009202
22 268-280 DiseaseOrPhenotypicFeature denotes sudden death MESH:D003645
23 396-404 ChemicalEntity denotes glycogen MESH:D006003
24 437-452 DiseaseOrPhenotypicFeature denotes Pompe's disease MESH:D006009
25 498-522 DiseaseOrPhenotypicFeature denotes infantile cardiomyopathy MESH:D009202

LitCoin-Disease-Tuning-1

Id Subject Object Predicate Lexical cue ID:
T1 30-42 DiseaseOrPhenotypicFeature denotes sudden death D003645
T2 51-78 DiseaseOrPhenotypicFeature denotes hypertrophic cardiomyopathy D002312
T3 82-97 DiseaseOrPhenotypicFeature denotes Pompe's disease D006009
T4 99-131 DiseaseOrPhenotypicFeature denotes Glycogen storage disease type II D006009
T5 133-148 DiseaseOrPhenotypicFeature denotes Pompe's disease D006009
T6 170-188 DiseaseOrPhenotypicFeature denotes metabolic disorder DISEASE
T7 221-226 DiseaseOrPhenotypicFeature denotes death D003643
T8 239-253 DiseaseOrPhenotypicFeature denotes cardiomyopathy D009202
T9 268-280 DiseaseOrPhenotypicFeature denotes sudden death D003645
T10 437-452 DiseaseOrPhenotypicFeature denotes Pompe's disease D006009
T11 508-522 DiseaseOrPhenotypicFeature denotes cardiomyopathy D009202

LitEisuke

Id Subject Object Predicate Lexical cue #label
T1 30-42 DiseaseOrPhenotypicFeature denotes sudden death D003645
T2 51-78 DiseaseOrPhenotypicFeature denotes hypertrophic cardiomyopathy D002312
T3 82-97 DiseaseOrPhenotypicFeature denotes Pompe's disease D006009
T4 99-131 DiseaseOrPhenotypicFeature denotes Glycogen storage disease type II D006009
T5 133-148 DiseaseOrPhenotypicFeature denotes Pompe's disease D006009
T6 170-188 DiseaseOrPhenotypicFeature denotes metabolic disorder DISEASE
T7 239-253 DiseaseOrPhenotypicFeature denotes cardiomyopathy D009202
T8 268-280 DiseaseOrPhenotypicFeature denotes sudden death D003645
T9 437-452 DiseaseOrPhenotypicFeature denotes Pompe's disease D006009
T10 508-522 DiseaseOrPhenotypicFeature denotes cardiomyopathy D009202

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-98 Sentence denotes An interesting case of infant sudden death: severe hypertrophic cardiomyopathy in Pompe's disease.
TextSentencer_T2 99-254 Sentence denotes Glycogen storage disease type II (Pompe's disease) is a rare inherited metabolic disorder, which often leads to infantile death from severe cardiomyopathy.
TextSentencer_T3 255-436 Sentence denotes This case of sudden death illustrates the features of the cardiac findings in the disorder, resulting from massive lysosomal accumulation of glycogen in the heart and other tissues.
TextSentencer_T4 437-523 Sentence denotes Pompe's disease should be considered in cases of unexplained infantile cardiomyopathy.
T1 0-98 Sentence denotes An interesting case of infant sudden death: severe hypertrophic cardiomyopathy in Pompe's disease.
T2 99-254 Sentence denotes Glycogen storage disease type II (Pompe's disease) is a rare inherited metabolic disorder, which often leads to infantile death from severe cardiomyopathy.
T3 255-436 Sentence denotes This case of sudden death illustrates the features of the cardiac findings in the disorder, resulting from massive lysosomal accumulation of glycogen in the heart and other tissues.
T4 437-523 Sentence denotes Pompe's disease should be considered in cases of unexplained infantile cardiomyopathy.

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 428-435 http://purl.obolibrary.org/obo/UBERON_0000479 denotes tissues
PD-UBERON-AE-B_T2 412-417 http://purl.obolibrary.org/obo/UBERON_0000948 denotes heart

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 51-78 HP:0001639 denotes hypertrophic cardiomyopathy
AB1 239-253 HP:0001638 denotes cardiomyopathy
AB2 508-522 HP:0001638 denotes cardiomyopathy

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 99-131 ORDO:365 denotes Glycogen storage disease type II

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 412-417 http://purl.obolibrary.org/obo/UBERON_0000948 denotes heart
PD-UBERON-AE-B_T2 428-435 http://purl.obolibrary.org/obo/UBERON_0000479 denotes tissues

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 170-188 HP_0001939 denotes metabolic disorder
T2 239-253 HP_0001638 denotes cardiomyopathy
T3 313-329 HP_0001627 denotes cardiac findings
T4 508-522 HP_0001638 denotes cardiomyopathy