TextAE configuration unavailable!

PubMed:11810296 JSONTXT

Annnotations TAB JSON ListView MergeView

FSU-PRGE

Id	Subject	Object	Predicate	Lexical cue
T1	82-86	protein	denotes	OPA1
T2	256-260	protein	denotes	OPA1
T3	411-415	protein	denotes	OPA1
T4	536-540	protein	denotes	OPA1
T5	1559-1563	protein	denotes	OPA1

PIR-corpus2

Id	Subject	Object	Predicate	Lexical cue
T1	82-86	protein	denotes	OPA1
T2	256-260	protein	denotes	OPA1
T3	411-415	protein	denotes	OPA1
T4	536-540	protein	denotes	OPA1
T5	1559-1563	protein	denotes	OPA1

DisGeNET5_gene_disease

Id	Subject	Object	Predicate	Lexical cue
11810296-0#82#86#gene4976	82-86	gene4976	denotes	OPA1
11810296-0#19#42#diseaseC0152136	19-42	diseaseC0152136	denotes	normal tension glaucoma
11810296-2#0#4#gene4976	256-260	gene4976	denotes	OPA1
11810296-2#155#159#gene4976	411-415	gene4976	denotes	OPA1
11810296-2#31#63#diseaseC0338508	287-319	diseaseC0338508	denotes	autosomal dominant optic atrophy
82#86#gene497619#42#diseaseC0152136	11810296-0#82#86#gene4976	11810296-0#19#42#diseaseC0152136	associated_with	OPA1,normal tension glaucoma
0#4#gene497631#63#diseaseC0338508	11810296-2#0#4#gene4976	11810296-2#31#63#diseaseC0338508	associated_with	OPA1,autosomal dominant optic atrophy
155#159#gene497631#63#diseaseC0338508	11810296-2#155#159#gene4976	11810296-2#31#63#diseaseC0338508	associated_with	OPA1,autosomal dominant optic atrophy

DisGeNET

Id	Subject	Object	Predicate	Lexical cue
T0	82-86	gene:4976	denotes	OPA1
T1	19-42	disease:C0152136	denotes	normal tension glaucoma
T2	82-86	gene:9968	denotes	OPA1
T3	19-42	disease:C0152136	denotes	normal tension glaucoma
T4	256-260	gene:9968	denotes	OPA1
T5	287-319	disease:C0338508	denotes	autosomal dominant optic atrophy
T6	256-260	gene:4976	denotes	OPA1
T7	287-319	disease:C0338508	denotes	autosomal dominant optic atrophy
T8	411-415	gene:4976	denotes	OPA1
T9	287-319	disease:C0338508	denotes	autosomal dominant optic atrophy
T10	411-415	gene:9968	denotes	OPA1
T11	363-366	disease:C0152136	denotes	NTG
T12	411-415	gene:4976	denotes	OPA1
T13	363-366	disease:C0152136	denotes	NTG
T14	411-415	gene:9968	denotes	OPA1
T15	287-319	disease:C0338508	denotes	autosomal dominant optic atrophy
T16	1559-1563	gene:4976	denotes	OPA1
T17	1589-1592	disease:C0152136	denotes	NTG
T18	1559-1563	gene:9968	denotes	OPA1
T19	1589-1592	disease:C0152136	denotes	NTG
R1	T0	T1	associated_with	OPA1,normal tension glaucoma
R2	T2	T3	associated_with	OPA1,normal tension glaucoma
R3	T4	T5	associated_with	OPA1,autosomal dominant optic atrophy
R4	T6	T7	associated_with	OPA1,autosomal dominant optic atrophy
R5	T8	T9	associated_with	OPA1,autosomal dominant optic atrophy
R6	T10	T11	associated_with	OPA1,NTG
R7	T12	T13	associated_with	OPA1,NTG
R8	T14	T15	associated_with	OPA1,autosomal dominant optic atrophy
R9	T16	T17	associated_with	OPA1,NTG
R10	T18	T19	associated_with	OPA1,NTG