PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25874378-5	2015	HHH syndrome is caused by impaired ornithine transport across the inner mitochondrial membrane due to mutations in SLC25A15 gene, which encodes for the mitochondrial ornithine carrier ORC1.	Ornithine	35-44	solute carrier family 25 member 15	Homo sapiens	115-123	
26589310-0	2016	Heterologous Expression in Yeast of Human Ornithine Carriers ORNT1 and ORNT2 and of ORNT1 Alleles Implicated in HHH Syndrome in Humans.	Ornithine	42-51	solute carrier family 25 member 15	Homo sapiens	61-66	
25874378-5	2015	HHH syndrome is caused by impaired ornithine transport across the inner mitochondrial membrane due to mutations in SLC25A15 gene, which encodes for the mitochondrial ornithine carrier ORC1.	Ornithine	166-175	solute carrier family 25 member 15	Homo sapiens	115-123	
24721342-2	2014	ORC1 is encoded by the SLC25A15 gene and catalyzes the transport of cytosolic ornithine into mitochondria in exchange for citrulline.	Ornithine	78-87	solute carrier family 25 member 15	Homo sapiens	23-31	
23430880-1	2012	The Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome is a disorder of the urea cycle and ornithine degradation pathway caused by mutations in the mitochondrial ornithine transporter, ORNT1 (SLC25A15).	Ornithine	9-18	solute carrier family 25 member 15	Homo sapiens	200-205	
23430880-1	2012	The Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome is a disorder of the urea cycle and ornithine degradation pathway caused by mutations in the mitochondrial ornithine transporter, ORNT1 (SLC25A15).	Ornithine	9-18	solute carrier family 25 member 15	Homo sapiens	207-215	
19287344-1	2009	The hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is a disorder of the urea cycle (UCD) and ornithine degradation pathway caused by mutations in the mitochondrial ornithine transporter (ORNT1).	Ornithine	9-18	solute carrier family 25 member 15	Homo sapiens	206-211	
18978333-1	2008	BACKGROUND: Hyperornithinaemia-hyperammonaemia-homocitrullinuria (HHH) syndrome (OMIM 238970) is caused by impaired ornithine transport across the inner mitochondrial membrane due to mutations in SLC25A15.	Ornithine	116-125	solute carrier family 25 member 15	Homo sapiens	196-204	
10369256-4	1999	ORNT1 expression restores ornithine metabolism in fibroblasts from patients with hyperammonaemia-hyperornithinaemia-homocitrullinuria (HHH) syndrome.	Ornithine	26-35	solute carrier family 25 member 15	Homo sapiens	0-5	
22649802-7	1993	DIAGNOSIS/TESTING: HHH syndrome is caused by mutation of SLC25A15, the gene that encodes ORNT1 (mitochondrial ornithine transporter 1), which is involved in the urea cycle and the ornithine degradation pathway.	Ornithine	110-119	solute carrier family 25 member 15	Homo sapiens	57-65	
22649802-7	1993	DIAGNOSIS/TESTING: HHH syndrome is caused by mutation of SLC25A15, the gene that encodes ORNT1 (mitochondrial ornithine transporter 1), which is involved in the urea cycle and the ornithine degradation pathway.	Ornithine	110-119	solute carrier family 25 member 15	Homo sapiens	89-94	
30403179-3	2018	In this study, we have investigated the effect of SLC25A15, which encodes the mitochondrial ornithine carrier 1, on melanoma progression.	Ornithine	92-101	solute carrier family 25 member 15	Homo sapiens	50-58