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PubMed:18796596 JSONTXT

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DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	915-921	gene:23435	denotes	TDP-43
T1	846-850	disease:C0751713	denotes	sIBM
T2	915-921	gene:23435	denotes	TDP-43
T3	881-891	disease:C0026848	denotes	myopathies
T4	915-921	gene:23435	denotes	TDP-43
T5	931-949	disease:C0010823	denotes	inclusion diseases
R1	T0	T1	associated_with	TDP-43,sIBM
R2	T2	T3	associated_with	TDP-43,myopathies
R3	T4	T5	associated_with	TDP-43,inclusion diseases

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
18796596-0#0#6#gene23435	0-6	gene23435	denotes	TDP-43
18796596-0#0#6#gene23435	0-6	gene23435	denotes	TDP-43
18796596-0#98#121#diseaseC0236642	98-121	diseaseC0236642	denotes	frontotemporal dementia
18796596-0#98#121#diseaseC0338451	98-121	diseaseC0338451	denotes	frontotemporal dementia
18796596-0#38#46#diseaseC0026848	38-46	diseaseC0026848	denotes	myopathy
18796596-2#43#69#gene7415	288-314	gene7415	denotes	valosin containing protein
18796596-2#71#74#gene7415	316-319	gene7415	denotes	VCP
18796596-2#112#120#diseaseC0026848	357-365	diseaseC0026848	denotes	myopathy
18796596-2#122#128#diseaseC1833662	367-373	diseaseC1833662	denotes	IBMPFD
18796596-3#53#59#gene23435	429-435	gene23435	denotes	TDP-43
18796596-3#74#80#diseaseC1833662	450-456	diseaseC1833662	denotes	IBMPFD
18796596-8#85#91#gene23435	915-921	gene23435	denotes	TDP-43
18796596-8#16#20#diseaseC0751713	846-850	diseaseC0751713	denotes	sIBM
18796596-8#101#119#diseaseC0010823	931-949	diseaseC0010823	denotes	inclusion diseases
0#6#gene2343598#121#diseaseC0236642	18796596-0#0#6#gene23435	18796596-0#98#121#diseaseC0236642	associated_with	TDP-43,frontotemporal dementia
0#6#gene2343598#121#diseaseC0338451	18796596-0#0#6#gene23435	18796596-0#98#121#diseaseC0338451	associated_with	TDP-43,frontotemporal dementia
0#6#gene2343538#46#diseaseC0026848	18796596-0#0#6#gene23435	18796596-0#38#46#diseaseC0026848	associated_with	TDP-43,myopathy
0#6#gene2343598#121#diseaseC0236642	18796596-0#0#6#gene23435	18796596-0#98#121#diseaseC0236642	associated_with	TDP-43,frontotemporal dementia
0#6#gene2343598#121#diseaseC0338451	18796596-0#0#6#gene23435	18796596-0#98#121#diseaseC0338451	associated_with	TDP-43,frontotemporal dementia
0#6#gene2343538#46#diseaseC0026848	18796596-0#0#6#gene23435	18796596-0#38#46#diseaseC0026848	associated_with	TDP-43,myopathy
43#69#gene7415112#120#diseaseC0026848	18796596-2#43#69#gene7415	18796596-2#112#120#diseaseC0026848	associated_with	valosin containing protein,myopathy
43#69#gene7415122#128#diseaseC1833662	18796596-2#43#69#gene7415	18796596-2#122#128#diseaseC1833662	associated_with	valosin containing protein,IBMPFD
71#74#gene7415112#120#diseaseC0026848	18796596-2#71#74#gene7415	18796596-2#112#120#diseaseC0026848	associated_with	VCP,myopathy
71#74#gene7415122#128#diseaseC1833662	18796596-2#71#74#gene7415	18796596-2#122#128#diseaseC1833662	associated_with	VCP,IBMPFD
53#59#gene2343574#80#diseaseC1833662	18796596-3#53#59#gene23435	18796596-3#74#80#diseaseC1833662	associated_with	TDP-43,IBMPFD
85#91#gene2343516#20#diseaseC0751713	18796596-8#85#91#gene23435	18796596-8#16#20#diseaseC0751713	associated_with	TDP-43,sIBM
85#91#gene23435101#119#diseaseC0010823	18796596-8#85#91#gene23435	18796596-8#101#119#diseaseC0010823	associated_with	TDP-43,inclusion diseases

PMID_GLOBAL

Id	Subject	Object	Predicate	Lexical cue	mondo_id
T1	38-46	DiseaseOrPhenotypicFeature	denotes	myopathy	0005336
T2	98-121	DiseaseOrPhenotypicFeature	denotes	frontotemporal dementia	0010857|0017276
T4	123-126	DiseaseOrPhenotypicFeature	denotes	TAR	0010121
T5	211-235	DiseaseOrPhenotypicFeature	denotes	frontotemporal dementias	0010857|0017276
T7	237-240	DiseaseOrPhenotypicFeature	denotes	FTD	0010857|0017276
T9	257-260	DiseaseOrPhenotypicFeature	denotes	FTD	0010857|0017276
T11	357-365	DiseaseOrPhenotypicFeature	denotes	myopathy	0005336
T12	367-373	DiseaseOrPhenotypicFeature	denotes	IBMPFD	0000507
T13	382-388	DiseaseOrPhenotypicFeature	denotes	IBMPFD	0000507
T14	450-456	DiseaseOrPhenotypicFeature	denotes	IBMPFD	0000507
T15	515-521	DiseaseOrPhenotypicFeature	denotes	IBMPFD	0000507
T16	658-690	DiseaseOrPhenotypicFeature	denotes	sporadic inclusion body myositis	0007827
T17	692-696	DiseaseOrPhenotypicFeature	denotes	sIBM	0007827
T18	710-716	DiseaseOrPhenotypicFeature	denotes	IBMPFD	0000507
T19	721-725	DiseaseOrPhenotypicFeature	denotes	sIBM	0007827
T20	816-819	DiseaseOrPhenotypicFeature	denotes	FTD	0010857|0017276
T22	846-850	DiseaseOrPhenotypicFeature	denotes	sIBM	0007827
T23	855-891	DiseaseOrPhenotypicFeature	denotes	hereditary inclusion body myopathies	0007827