PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27271685-1	2016	Expansion of the polyglutamine (polyQ) track of the Huntingtin (HTT) protein above 36 is associated with a sharply enhanced risk of Huntington"s disease (HD).	polyglutamine	17-30	huntingtin	Rattus norvegicus	52-62	
27271685-1	2016	Expansion of the polyglutamine (polyQ) track of the Huntingtin (HTT) protein above 36 is associated with a sharply enhanced risk of Huntington"s disease (HD).	polyglutamine	17-30	huntingtin	Rattus norvegicus	64-67	
27271685-1	2016	Expansion of the polyglutamine (polyQ) track of the Huntingtin (HTT) protein above 36 is associated with a sharply enhanced risk of Huntington"s disease (HD).	polyglutamine	32-37	huntingtin	Rattus norvegicus	52-62	
27271685-1	2016	Expansion of the polyglutamine (polyQ) track of the Huntingtin (HTT) protein above 36 is associated with a sharply enhanced risk of Huntington"s disease (HD).	polyglutamine	32-37	huntingtin	Rattus norvegicus	64-67	
27271685-3	2016	One hypothesis is that polyQ expansion induces an alternative, toxic conformation in the HTT exon1 monomer.	polyglutamine	23-28	huntingtin	Rattus norvegicus	89-92	
27271685-7	2016	We find that, in vitro, mutant HTT exon1 peptides engage in polyQ repeat length dependent dimer and tetramer formation, followed by time dependent formation of diffusible spherical and fibrillar oligomers and finally by larger, sedimentable amyloid fibrils.	polyglutamine	60-65	huntingtin	Rattus norvegicus	31-34