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PubMed:18487244 JSONTXT

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PMID_GLOBAL

Id	Subject	Object	Predicate	Lexical cue	mondo_id
T1	316-331	DiseaseOrPhenotypicFeature	denotes	Alpers syndrome	0008758
T2	402-422	DiseaseOrPhenotypicFeature	denotes	hepatoencephalopathy	0001711
T3	1041-1049	DiseaseOrPhenotypicFeature	denotes	Epilepsy	0005027
T4	1057-1074	DiseaseOrPhenotypicFeature	denotes	movement disorder	0005395

TEST-DiseaseOrPhenotypicFeature

Id	Subject	Object	Predicate	Lexical cue	#label
T1	316-331	DiseaseOrPhenotypicFeature	denotes	Alpers syndrome	D002549
T2	1041-1049	DiseaseOrPhenotypicFeature	denotes	Epilepsy	D004827
T3	1057-1074	DiseaseOrPhenotypicFeature	denotes	movement disorder	D009069

TEST-ChemicalEntity

Id	Subject	Object	Predicate	Lexical cue	ID:
T1	901-912	ChemicalEntity	denotes	exonuclease	D005092
T2	1453-1464	ChemicalEntity	denotes	exonuclease	D005092
T3	1541-1552	ChemicalEntity	denotes	exonuclease	D005092
T4	1649-1664	ChemicalEntity	denotes	DNA polymerases	D004259

TEST-OrganismTaxon

Id	Subject	Object	Predicate	Lexical cue
T1	59-67	OrganismTaxon	denotes	patients
T2	541-549	OrganismTaxon	denotes	Patients
T3	702-710	OrganismTaxon	denotes	patients
T4	805-813	OrganismTaxon	denotes	patients
T5	957-965	OrganismTaxon	denotes	patients
T6	1328-1335	OrganismTaxon	denotes	patient
T7	1638-1648	OrganismTaxon	denotes	eukaryotic

Test-GeneOrGeneProduct

Id	Subject	Object	Predicate	Lexical cue
T1	73-78	GeneOrGeneProduct	denotes	POLG1
T2	216-241	GeneOrGeneProduct	denotes	catalytic (alpha) subunit
T3	293-298	GeneOrGeneProduct	denotes	POLG1
T4	354-359	GeneOrGeneProduct	denotes	POLG1
T5	736-742	GeneOrGeneProduct	denotes	mosaic
T6	858-863	GeneOrGeneProduct	denotes	POLG1
T7	901-912	GeneOrGeneProduct	denotes	exonuclease
T8	1200-1206	GeneOrGeneProduct	denotes	mosaic
T9	1415-1420	GeneOrGeneProduct	denotes	POLG1
T10	1453-1464	GeneOrGeneProduct	denotes	exonuclease
T11	1500-1505	GeneOrGeneProduct	denotes	POLG1
T12	1535-1552	GeneOrGeneProduct	denotes	3'-5' exonuclease
T13	1638-1648	GeneOrGeneProduct	denotes	eukaryotic
T14	1649-1664	GeneOrGeneProduct	denotes	DNA polymerases

Test-merged-2

Id	Subject	Object	Predicate	Lexical cue	#label	ID:
T87437	901-912	ChemicalEntity	denotes	exonuclease		D005092
T75687	1453-1464	ChemicalEntity	denotes	exonuclease		D005092
T53121	1541-1552	ChemicalEntity	denotes	exonuclease		D005092
T90129	1649-1664	ChemicalEntity	denotes	DNA polymerases		D004259
T48705	73-78	GeneOrGeneProduct	denotes	POLG1
T37351	216-241	GeneOrGeneProduct	denotes	catalytic (alpha) subunit
T66708	293-298	GeneOrGeneProduct	denotes	POLG1
T85904	354-359	GeneOrGeneProduct	denotes	POLG1
T39144	736-742	GeneOrGeneProduct	denotes	mosaic
T22212	858-863	GeneOrGeneProduct	denotes	POLG1
T92825	901-912	GeneOrGeneProduct	denotes	exonuclease
T8	1200-1206	GeneOrGeneProduct	denotes	mosaic
T9	1415-1420	GeneOrGeneProduct	denotes	POLG1
T10	1453-1464	GeneOrGeneProduct	denotes	exonuclease
T11	1500-1505	GeneOrGeneProduct	denotes	POLG1
T12	1535-1552	GeneOrGeneProduct	denotes	3'-5' exonuclease
T13	1638-1648	GeneOrGeneProduct	denotes	eukaryotic
T14	1649-1664	GeneOrGeneProduct	denotes	DNA polymerases
T4569	59-67	OrganismTaxon	denotes	patients
T45117	541-549	OrganismTaxon	denotes	Patients
T72129	702-710	OrganismTaxon	denotes	patients
T4	805-813	OrganismTaxon	denotes	patients
T5	957-965	OrganismTaxon	denotes	patients
T6	1328-1335	OrganismTaxon	denotes	patient
T7	1638-1648	OrganismTaxon	denotes	eukaryotic
T1	316-331	DiseaseOrPhenotypicFeature	denotes	Alpers syndrome	D002549
T2	1041-1049	DiseaseOrPhenotypicFeature	denotes	Epilepsy	D004827
T3	1057-1074	DiseaseOrPhenotypicFeature	denotes	movement disorder	D009069

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	73-78	gene:5428	denotes	POLG1
T1	0-30	disease:C0342782	denotes	Depletion of mitochondrial DNA
R1	T0	T1	associated_with	POLG1,Depletion of mitochondrial DNA

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
18487244-0#73#78#gene5428	73-78	gene5428	denotes	POLG1
18487244-0#0#30#diseaseC0342782	0-30	diseaseC0342782	denotes	Depletion of mitochondrial DNA
73#78#gene54280#30#diseaseC0342782	18487244-0#73#78#gene5428	18487244-0#0#30#diseaseC0342782	associated_with	POLG1,Depletion of mitochondrial DNA