PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19681162-1	2009	Dentatorubral-pallidoluysian atrophy (DRPLA) is a dominant hereditary neurodegenerative disorder caused by the expansion of a poly-glutamine (poly-Q) repeat in Atrophin-1 protein.	polyglutamine	126-140	atrophin 1	Mus musculus	38-43	
19681162-1	2009	Dentatorubral-pallidoluysian atrophy (DRPLA) is a dominant hereditary neurodegenerative disorder caused by the expansion of a poly-glutamine (poly-Q) repeat in Atrophin-1 protein.	polyglutamine	126-140	atrophin 1	Mus musculus	160-170	
19681162-1	2009	Dentatorubral-pallidoluysian atrophy (DRPLA) is a dominant hereditary neurodegenerative disorder caused by the expansion of a poly-glutamine (poly-Q) repeat in Atrophin-1 protein.	polyglutamine	142-148	atrophin 1	Mus musculus	38-43	
19681162-1	2009	Dentatorubral-pallidoluysian atrophy (DRPLA) is a dominant hereditary neurodegenerative disorder caused by the expansion of a poly-glutamine (poly-Q) repeat in Atrophin-1 protein.	polyglutamine	142-148	atrophin 1	Mus musculus	160-170	
19681162-7	2009	These results support the model that poly-Q expanded Atrophin-1 proteins cause DRPLA in a manner independent of any functional interaction with wild-type Atrophin-1 proteins.	polyglutamine	37-43	atrophin 1	Mus musculus	53-63	
19681162-7	2009	These results support the model that poly-Q expanded Atrophin-1 proteins cause DRPLA in a manner independent of any functional interaction with wild-type Atrophin-1 proteins.	polyglutamine	37-43	atrophin 1	Mus musculus	79-84