PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25852896-2	2014	GS is caused by mutations in the SLC12A3 gene encoding the Na(+)-Cl(-) co-transporter of the distal convoluted tubule (NCCT) and tends to be associated with a milder salt-losing phenotype.	Salts	166-170	solute carrier family 12 member 3	Homo sapiens	33-40	
25852896-2	2014	GS is caused by mutations in the SLC12A3 gene encoding the Na(+)-Cl(-) co-transporter of the distal convoluted tubule (NCCT) and tends to be associated with a milder salt-losing phenotype.	Salts	166-170	solute carrier family 12 member 3	Homo sapiens	119-123	
25852896-3	2014	We describe two female siblings presenting in infancy with a severe salt-losing tubulopathy and failure to thrive due to compound heterozygous mutations in the SLC12A3 gene encoding the NCCT.	Salts	68-72	solute carrier family 12 member 3	Homo sapiens	160-167	
25852896-3	2014	We describe two female siblings presenting in infancy with a severe salt-losing tubulopathy and failure to thrive due to compound heterozygous mutations in the SLC12A3 gene encoding the NCCT.	Salts	68-72	solute carrier family 12 member 3	Homo sapiens	186-190