PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
18418675-1	2008	Spinocerebellar ataxia type 7 (SCA7) is unique among CAG/polyglutamine (polyQ) repeat diseases due to dramatic intergenerational instability in repeat length and an associated cone-rod dystrophy retinal degeneration phenotype.	polyglutamine	57-70	ataxin 7	Homo sapiens	0-29	
18418675-1	2008	Spinocerebellar ataxia type 7 (SCA7) is unique among CAG/polyglutamine (polyQ) repeat diseases due to dramatic intergenerational instability in repeat length and an associated cone-rod dystrophy retinal degeneration phenotype.	polyglutamine	57-70	ataxin 7	Homo sapiens	31-35	
18418675-1	2008	Spinocerebellar ataxia type 7 (SCA7) is unique among CAG/polyglutamine (polyQ) repeat diseases due to dramatic intergenerational instability in repeat length and an associated cone-rod dystrophy retinal degeneration phenotype.	polyglutamine	72-77	ataxin 7	Homo sapiens	0-29	
18418675-1	2008	Spinocerebellar ataxia type 7 (SCA7) is unique among CAG/polyglutamine (polyQ) repeat diseases due to dramatic intergenerational instability in repeat length and an associated cone-rod dystrophy retinal degeneration phenotype.	polyglutamine	72-77	ataxin 7	Homo sapiens	31-35	
18418675-2	2008	SCA7 is caused by a polyQ expansion in the protein ataxin-7.	polyglutamine	20-25	ataxin 7	Homo sapiens	0-4	
18418675-2	2008	SCA7 is caused by a polyQ expansion in the protein ataxin-7.	polyglutamine	20-25	ataxin 7	Homo sapiens	51-59	
18418675-4	2008	Several potential mechanisms for the molecular pathogenesis of polyQ-expanded ataxin-7 have been suggested.	polyglutamine	63-68	ataxin 7	Homo sapiens	78-86	
18418675-5	2008	These include, but are not limited to, alteration of endogenous ataxin-7 function, abnormal processing and stability of polyQ ataxin-7, and alteration of transcriptional regulation via interaction of polyQ-expanded ataxin-7 with other transcriptional regulators.	polyglutamine	120-125	ataxin 7	Homo sapiens	126-134	
18418675-5	2008	These include, but are not limited to, alteration of endogenous ataxin-7 function, abnormal processing and stability of polyQ ataxin-7, and alteration of transcriptional regulation via interaction of polyQ-expanded ataxin-7 with other transcriptional regulators.	polyglutamine	120-125	ataxin 7	Homo sapiens	126-134	
18418675-7	2008	PolyQ-expanded ataxin-7 can cause non-cell autonomous neurodegeneration in cerebellar Purkinje cells.	polyglutamine	0-5	ataxin 7	Homo sapiens	15-23