PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15100168-4	2004	When expressed in Xenopus laevis oocytes, mOat3 mediated the uptake of p-aminohippuric acid and estron sulfate (ES).	p-Aminohippuric Acid	71-91	solute carrier family 22 (organic anion transporter), member 8	Mus musculus	42-47	
15944205-6	2005	Six tryptophan metabolites, including the bioactive substances KYNA, XA, and the serotonin metabolite 5-hydroxyindol acetate inhibited [(3)H]p-aminohippurate (PAH) or 6-carboxyfluorescein (6-CF) uptake by 50-85%, demonstrating that these compounds interact with OAT1 as well as with OAT3.	p-Aminohippuric Acid	159-162	solute carrier family 22 (organic anion transporter), member 8	Mus musculus	283-287	
15075193-3	2004	We recently generated an organic anion transporter 3- (Oat3)-null mouse, which exhibited loss of PAH, estrone sulfate, and taurocholate transport in kidney and of fluorescein (FL) transport in choroid plexus.	p-Aminohippuric Acid	97-100	solute carrier family 22 (organic anion transporter), member 8	Mus musculus	25-59	
15075193-5	2004	Mediated transport of PAH and FL was essentially abolished in tissue from Oat3-null mice.	p-Aminohippuric Acid	22-25	solute carrier family 22 (organic anion transporter), member 8	Mus musculus	74-78	
15075193-7	2004	For PAH, FL, and estrone sulfate, all Oat3-mediated transport was Na dependent.	p-Aminohippuric Acid	4-7	solute carrier family 22 (organic anion transporter), member 8	Mus musculus	38-42