PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24035636-1	2013	Autosomal recessive cutis laxa type 2B (ARCL2B; OMIM # 612940) is a segmental progeroid disorder caused by mutations in PYCR1 encoding pyrroline-5-carboxylate reductase 1, which is part of the conserved proline de novo synthesis pathway.	Proline	203-210	pyrroline-5-carboxylate reductase 1	Homo sapiens	0-38	
24035636-1	2013	Autosomal recessive cutis laxa type 2B (ARCL2B; OMIM # 612940) is a segmental progeroid disorder caused by mutations in PYCR1 encoding pyrroline-5-carboxylate reductase 1, which is part of the conserved proline de novo synthesis pathway.	Proline	203-210	pyrroline-5-carboxylate reductase 1	Homo sapiens	40-46	
24035636-1	2013	Autosomal recessive cutis laxa type 2B (ARCL2B; OMIM # 612940) is a segmental progeroid disorder caused by mutations in PYCR1 encoding pyrroline-5-carboxylate reductase 1, which is part of the conserved proline de novo synthesis pathway.	Proline	203-210	pyrroline-5-carboxylate reductase 1	Homo sapiens	120-125	
24035636-1	2013	Autosomal recessive cutis laxa type 2B (ARCL2B; OMIM # 612940) is a segmental progeroid disorder caused by mutations in PYCR1 encoding pyrroline-5-carboxylate reductase 1, which is part of the conserved proline de novo synthesis pathway.	Proline	203-210	pyrroline-5-carboxylate reductase 1	Homo sapiens	135-170