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PubMed:17391797 JSONTXT

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TEST-DiseaseOrPhenotypicFeature

Id	Subject	Object	Predicate	Lexical cue	#label
T1	121-125	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T2	216-244	DiseaseOrPhenotypicFeature	denotes	nonalcoholic steatohepatitis	D065626
T3	246-250	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T4	599-603	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T5	663-667	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T6	883-887	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T7	1005-1009	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T8	1062-1066	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T9	1135-1140	DiseaseOrPhenotypicFeature	denotes	obese	DISEASE
T10	1372-1376	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T11	1420-1424	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T12	1442-1447	DiseaseOrPhenotypicFeature	denotes	obese	DISEASE
T13	1514-1518	DiseaseOrPhenotypicFeature	denotes	NASH	D065626

TEST-ChemicalEntity

Id	Subject	Object	Predicate	Lexical cue	ID:
T1	4-48	ChemicalEntity	denotes	phosphatidylethanolamine N-methyltransferase	D050918
T2	332-376	ChemicalEntity	denotes	phosphatidylethanolamine N-methyltransferase	D050918
T3	378-382	ChemicalEntity	denotes	PEMT	D050918
T4	417-441	ChemicalEntity	denotes	phosphatidylethanolamine	C483858|http://purl.obolibrary.org/obo/CHEBI_16038
T6	445-464	ChemicalEntity	denotes	phosphatidylcholine	D010713|http://purl.obolibrary.org/obo/CHEBI_64482
T8	561-565	ChemicalEntity	denotes	PEMT	D050918
T9	838-842	ChemicalEntity	denotes	PEMT	D050918
T10	1259-1263	ChemicalEntity	denotes	PEMT	D050918
T11	1299-1303	ChemicalEntity	denotes	PEMT	D050918
T12	1482-1486	ChemicalEntity	denotes	PEMT	D050918

TEST-OrganismTaxon

Id	Subject	Object	Predicate	Lexical cue
T1	635-643	OrganismTaxon	denotes	patients
T2	888-896	OrganismTaxon	denotes	patients
T3	1010-1018	OrganismTaxon	denotes	patients
T4	1067-1075	OrganismTaxon	denotes	patients
T5	1141-1149	OrganismTaxon	denotes	patients
T6	1425-1433	OrganismTaxon	denotes	patients

Test-SequenceVariant

Id	Subject	Object	Predicate	Lexical cue
T1	54-59	SequenceVariant	denotes	V175M
T2	306-315	SequenceVariant	denotes	Val175Met
T3	531-540	SequenceVariant	denotes	Val175Met
T4	806-815	SequenceVariant	denotes	Val175Met
T5	951-960	SequenceVariant	denotes	Val175Met
T6	1208-1217	SequenceVariant	denotes	Val175Met
T7	1278-1287	SequenceVariant	denotes	Val175Met
T8	1461-1470	SequenceVariant	denotes	Val175Met

Test-GeneOrGeneProduct

Id	Subject	Object	Predicate	Lexical cue
T1	4-48	GeneOrGeneProduct	denotes	phosphatidylethanolamine N-methyltransferase
T2	332-376	GeneOrGeneProduct	denotes	phosphatidylethanolamine N-methyltransferase
T3	378-382	GeneOrGeneProduct	denotes	PEMT
T4	417-441	GeneOrGeneProduct	denotes	phosphatidylethanolamine
T5	445-464	GeneOrGeneProduct	denotes	phosphatidylcholine
T6	561-565	GeneOrGeneProduct	denotes	PEMT
T7	838-842	GeneOrGeneProduct	denotes	PEMT
T8	1259-1263	GeneOrGeneProduct	denotes	PEMT
T9	1299-1303	GeneOrGeneProduct	denotes	PEMT
T10	1482-1486	GeneOrGeneProduct	denotes	PEMT

Test-merged-2

Id	Subject	Object	Predicate	Lexical cue	#label	ID:
T92178	54-59	SequenceVariant	denotes	V175M
T80384	306-315	SequenceVariant	denotes	Val175Met
T63808	531-540	SequenceVariant	denotes	Val175Met
T31129	806-815	SequenceVariant	denotes	Val175Met
T42884	951-960	SequenceVariant	denotes	Val175Met
T3132	1208-1217	SequenceVariant	denotes	Val175Met
T10091	1278-1287	SequenceVariant	denotes	Val175Met
T94115	1461-1470	SequenceVariant	denotes	Val175Met
T6716	4-48	ChemicalEntity	denotes	phosphatidylethanolamine N-methyltransferase		D050918
T563	332-376	ChemicalEntity	denotes	phosphatidylethanolamine N-methyltransferase		D050918
T17622	378-382	ChemicalEntity	denotes	PEMT		D050918
T30554	417-441	ChemicalEntity	denotes	phosphatidylethanolamine		C483858|http://purl.obolibrary.org/obo/CHEBI_16038
T87131	445-464	ChemicalEntity	denotes	phosphatidylcholine		D010713|http://purl.obolibrary.org/obo/CHEBI_64482
T89112	561-565	ChemicalEntity	denotes	PEMT		D050918
T10843	838-842	ChemicalEntity	denotes	PEMT		D050918
T74175	1259-1263	ChemicalEntity	denotes	PEMT		D050918
T76041	1299-1303	ChemicalEntity	denotes	PEMT		D050918
T56537	1482-1486	ChemicalEntity	denotes	PEMT		D050918
T14993	4-48	GeneOrGeneProduct	denotes	phosphatidylethanolamine N-methyltransferase
T8687	332-376	GeneOrGeneProduct	denotes	phosphatidylethanolamine N-methyltransferase
T36108	378-382	GeneOrGeneProduct	denotes	PEMT
T13751	417-441	GeneOrGeneProduct	denotes	phosphatidylethanolamine
T77480	445-464	GeneOrGeneProduct	denotes	phosphatidylcholine
T23967	561-565	GeneOrGeneProduct	denotes	PEMT
T10540	838-842	GeneOrGeneProduct	denotes	PEMT
T250	1259-1263	GeneOrGeneProduct	denotes	PEMT
T34997	1299-1303	GeneOrGeneProduct	denotes	PEMT
T98177	1482-1486	GeneOrGeneProduct	denotes	PEMT
T49664	635-643	OrganismTaxon	denotes	patients
T85854	888-896	OrganismTaxon	denotes	patients
T3882	1010-1018	OrganismTaxon	denotes	patients
T41710	1067-1075	OrganismTaxon	denotes	patients
T85902	1141-1149	OrganismTaxon	denotes	patients
T95853	1425-1433	OrganismTaxon	denotes	patients
T1	121-125	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T2	216-244	DiseaseOrPhenotypicFeature	denotes	nonalcoholic steatohepatitis	D065626
T3	246-250	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T4	599-603	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T5	663-667	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T6	883-887	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T7	1005-1009	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T8	1062-1066	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T9	1135-1140	DiseaseOrPhenotypicFeature	denotes	obese	DISEASE
T10	1372-1376	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T11	1420-1424	DiseaseOrPhenotypicFeature	denotes	NASH	D065626
T12	1442-1447	DiseaseOrPhenotypicFeature	denotes	obese	DISEASE
T13	1514-1518	DiseaseOrPhenotypicFeature	denotes	NASH	D065626

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	561-565	gene:10400	denotes	PEMT
T1	599-603	disease:C3241937	denotes	NASH
T2	1299-1303	gene:10400	denotes	PEMT
T3	1514-1518	disease:C3241937	denotes	NASH
T4	1299-1303	gene:10400	denotes	PEMT
T5	1420-1424	disease:C3241937	denotes	NASH
T6	1299-1303	gene:10400	denotes	PEMT
T7	1372-1376	disease:C3241937	denotes	NASH
T8	1482-1486	gene:10400	denotes	PEMT
T9	1372-1376	disease:C3241937	denotes	NASH
T10	1482-1486	gene:10400	denotes	PEMT
T11	1442-1447	disease:C0028754	denotes	obese
T12	1482-1486	gene:10400	denotes	PEMT
T13	1514-1518	disease:C3241937	denotes	NASH
R1	T0	T1	associated_with	PEMT,NASH
R2	T2	T3	associated_with	PEMT,NASH
R3	T4	T5	associated_with	PEMT,NASH
R4	T6	T7	associated_with	PEMT,NASH
R5	T8	T9	associated_with	PEMT,NASH
R6	T10	T11	associated_with	PEMT,obese
R7	T12	T13	associated_with	PEMT,NASH

DisGeNET5_variant_disease

Id	Subject	Object	Predicate	Lexical cue
17391797-0#54#59#geners7946	54-59	geners7946	denotes	V175M
17391797-0#121#125#diseaseC3241937	121-125	diseaseC3241937	denotes	NASH
17391797-7#183#192#geners7946	1461-1470	geners7946	denotes	Val175Met
17391797-7#0#9#geners7946	1278-1287	geners7946	denotes	Val175Met
17391797-7#164#169#diseaseC0028754	1442-1447	diseaseC0028754	denotes	obese
54#59#geners7946121#125#diseaseC3241937	17391797-0#54#59#geners7946	17391797-0#121#125#diseaseC3241937	associated_with	V175M,NASH
183#192#geners7946164#169#diseaseC0028754	17391797-7#183#192#geners7946	17391797-7#164#169#diseaseC0028754	associated_with	Val175Met,obese
0#9#geners7946164#169#diseaseC0028754	17391797-7#0#9#geners7946	17391797-7#164#169#diseaseC0028754	associated_with	Val175Met,obese

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
17391797-0#4#48#gene10400	4-48	gene10400	denotes	phosphatidylethanolamine N-methyltransferase
17391797-0#121#125#diseaseC3241937	121-125	diseaseC3241937	denotes	NASH
17391797-7#21#25#gene10400	1299-1303	gene10400	denotes	PEMT
17391797-7#204#208#gene10400	1482-1486	gene10400	denotes	PEMT
17391797-7#164#169#diseaseC0028754	1442-1447	diseaseC0028754	denotes	obese
4#48#gene10400121#125#diseaseC3241937	17391797-0#4#48#gene10400	17391797-0#121#125#diseaseC3241937	associated_with	phosphatidylethanolamine N-methyltransferase,NASH
21#25#gene10400164#169#diseaseC0028754	17391797-7#21#25#gene10400	17391797-7#164#169#diseaseC0028754	associated_with	PEMT,obese
204#208#gene10400164#169#diseaseC0028754	17391797-7#204#208#gene10400	17391797-7#164#169#diseaseC0028754	associated_with	PEMT,obese

tmVarCorpus

Id	Subject	Object	Predicate	Lexical cue
T1	54-59	ProteinMutation:p|SUB|V|175|M	denotes	V175M
T2	306-315	ProteinMutation:p|SUB|V|175|M	denotes	Val175Met
T3	531-540	ProteinMutation:p|SUB|V|175|M	denotes	Val175Met
T4	806-815	ProteinMutation:p|SUB|V|175|M	denotes	Val175Met
T5	951-960	ProteinMutation:p|SUB|V|175|M	denotes	Val175Met
T6	1208-1217	ProteinMutation:p|SUB|V|175|M	denotes	Val175Met
T7	1278-1287	ProteinMutation:p|SUB|V|175|M	denotes	Val175Met
T8	1461-1470	ProteinMutation:p|SUB|V|175|M	denotes	Val175Met