PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24367279-1	2013	Amyloid-like inclusions have been associated with Huntington"s disease (HD), which is caused by expanded polyglutamine repeats in the Huntingtin protein.	polyglutamine	105-118	huntingtin	Drosophila melanogaster	134-144	
24367279-3	2013	We have generated a Drosophila model of cardiac amyloidosis that exhibits accumulation of PolyQ aggregates and oxidative stress in myocardial cells, upon heart-specific expression of Huntingtin protein fragments (Htt-PolyQ) with disease-causing poly-glutamine repeats (PolyQ-46, PolyQ-72, and PolyQ-102).	polyglutamine	245-259	huntingtin	Drosophila melanogaster	183-193	
24367279-3	2013	We have generated a Drosophila model of cardiac amyloidosis that exhibits accumulation of PolyQ aggregates and oxidative stress in myocardial cells, upon heart-specific expression of Huntingtin protein fragments (Htt-PolyQ) with disease-causing poly-glutamine repeats (PolyQ-46, PolyQ-72, and PolyQ-102).	polyglutamine	245-259	huntingtin	Drosophila melanogaster	213-216	
24367279-4	2013	Cardiac expression of GFP-tagged Htt-PolyQs resulted in PolyQ length-dependent functional defects that included increased incidence of arrhythmias and extreme cardiac dilation, accompanied by a significant decrease in contractility.	polyglutamine	37-43	huntingtin	Drosophila melanogaster	33-36	
24367279-4	2013	Cardiac expression of GFP-tagged Htt-PolyQs resulted in PolyQ length-dependent functional defects that included increased incidence of arrhythmias and extreme cardiac dilation, accompanied by a significant decrease in contractility.	polyglutamine	37-42	huntingtin	Drosophila melanogaster	33-36