PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15932940-0	2005	Polyglutamine-expanded ataxin-7 inhibits STAGA histone acetyltransferase activity to produce retinal degeneration.	polyglutamine	0-13	ataxin 7	Homo sapiens	23-31	
15932940-1	2005	Spinocerebellar ataxia type 7 (SCA7) is characterized by cone-rod dystrophy retinal degeneration and is caused by a polyglutamine [poly(Q)] expansion within ataxin-7, a protein of previously unknown function.	polyglutamine	116-129	ataxin 7	Homo sapiens	0-29	
15932940-1	2005	Spinocerebellar ataxia type 7 (SCA7) is characterized by cone-rod dystrophy retinal degeneration and is caused by a polyglutamine [poly(Q)] expansion within ataxin-7, a protein of previously unknown function.	polyglutamine	116-129	ataxin 7	Homo sapiens	31-35	
15932940-1	2005	Spinocerebellar ataxia type 7 (SCA7) is characterized by cone-rod dystrophy retinal degeneration and is caused by a polyglutamine [poly(Q)] expansion within ataxin-7, a protein of previously unknown function.	polyglutamine	116-129	ataxin 7	Homo sapiens	157-165	
15932940-1	2005	Spinocerebellar ataxia type 7 (SCA7) is characterized by cone-rod dystrophy retinal degeneration and is caused by a polyglutamine [poly(Q)] expansion within ataxin-7, a protein of previously unknown function.	polyglutamine	131-138	ataxin 7	Homo sapiens	0-29	
15932940-1	2005	Spinocerebellar ataxia type 7 (SCA7) is characterized by cone-rod dystrophy retinal degeneration and is caused by a polyglutamine [poly(Q)] expansion within ataxin-7, a protein of previously unknown function.	polyglutamine	131-138	ataxin 7	Homo sapiens	31-35	
15932940-1	2005	Spinocerebellar ataxia type 7 (SCA7) is characterized by cone-rod dystrophy retinal degeneration and is caused by a polyglutamine [poly(Q)] expansion within ataxin-7, a protein of previously unknown function.	polyglutamine	131-138	ataxin 7	Homo sapiens	157-165