PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24296361-1	2014	Huntington"s disease is an inherited disorder caused by expanded stretch of consecutive trinucleotides (cytosine-adenosine-guanine, CAG) within the first exon of the huntingtin (HTT) gene on chromosome 4 (p16.3).	trinucleotides	88-102	huntingtin	Homo sapiens	166-176	
35275350-1	2022	Huntington"s disease (HD) is a genetic neurodegenerative progressive and fatal disease characterized by motor disorder, cognitive impairment, and behavioral problems, caused by expanded repeats of CAG trinucleotides in the HTT gene.	trinucleotides	201-215	huntingtin	Homo sapiens	223-226	
32878904-1	2020	BACKGROUND: Huntington"s disease (HD)(MIM:143100) is an severe autosomal dominant neurodegenerative disease caused by the dynamic expansion of CAG trinucleotides (> 35) in the HTT gene [Genomic Coordinates- (GRCh38):4:3,074,680-3,243,959].	trinucleotides	147-161	huntingtin	Homo sapiens	176-179	
32067426-1	2020	BACKGROUND: Huntington disease (HD) (MIM: 143100) is a severe autosomal dominant neurodegenerative disease caused by the expansion of CAG trinucleotides (>35) in the HTT.	trinucleotides	138-152	huntingtin	Homo sapiens	166-169	
24296361-1	2014	Huntington"s disease is an inherited disorder caused by expanded stretch of consecutive trinucleotides (cytosine-adenosine-guanine, CAG) within the first exon of the huntingtin (HTT) gene on chromosome 4 (p16.3).	trinucleotides	88-102	huntingtin	Homo sapiens	178-181	
10363492-4	1999	The gene (IT15) is localized in the short arm of chromosome 4 in the telemaric region 4p16.3 and it is known that the mutation is produced by an increase in the number of trinucleotides CAG (glutamine) localized in the 5" end of the gene, in the first exon.	trinucleotides	171-185	huntingtin	Homo sapiens	10-14