PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
32213296-1	2020	Marfan syndrome (MFS) is a connective tissue disorder caused by mutations of the FBN1 gene encoding fibrillin-1, which leads to overexpression of transforming growth factor-beta, increased hyaluronan deposition, and matrix metalloproteinase activity in the media of the aorta and other muscular arteries.	Hyaluronic Acid	189-199	fibrillin 1	Homo sapiens	81-85	
32213296-1	2020	Marfan syndrome (MFS) is a connective tissue disorder caused by mutations of the FBN1 gene encoding fibrillin-1, which leads to overexpression of transforming growth factor-beta, increased hyaluronan deposition, and matrix metalloproteinase activity in the media of the aorta and other muscular arteries.	Hyaluronic Acid	189-199	fibrillin 1	Homo sapiens	100-111