PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
12502708-4	2003	Verapamil and cyclosporin A, blockers of the multidrug resistance-associated protein, decreased UVA-induced GSH efflux.	Cyclosporine	14-27	ATP binding cassette subfamily C member 3	Homo sapiens	45-84	
7493917-0	1995	Multidrug resistance-associated protein-mediated multidrug resistance modulated by cyclosporin A in a human bladder cancer cell line.	Cyclosporine	83-96	ATP binding cassette subfamily C member 3	Homo sapiens	0-39	
11189941-8	2000	These results suggest that both Tc-MIBI and Tc-Tfos are substrates for the MRP transporter and that PSC833, Vrp, CsA and BSO but not GG918 can inhibit MRP activity.	Cyclosporine	113-116	ATP binding cassette subfamily C member 3	Homo sapiens	75-78	
11189941-8	2000	These results suggest that both Tc-MIBI and Tc-Tfos are substrates for the MRP transporter and that PSC833, Vrp, CsA and BSO but not GG918 can inhibit MRP activity.	Cyclosporine	113-116	ATP binding cassette subfamily C member 3	Homo sapiens	151-154	
9506530-6	1998	The P-glycoprotein-mediated multidrug resistance (MDR)-reversing agents verapamil, cyclosporin A, quinidine, sodium orthovanadate and tamoxifen significantly increased dox fluorescence at this depth, whereas genistein, indomethacin, probenecid and brefeldin A, which reverse multidrug-resistance-associated protein (MRP) function, exerted no effect.	Cyclosporine	83-96	ATP binding cassette subfamily C member 3	Homo sapiens	275-314	
9506530-6	1998	The P-glycoprotein-mediated multidrug resistance (MDR)-reversing agents verapamil, cyclosporin A, quinidine, sodium orthovanadate and tamoxifen significantly increased dox fluorescence at this depth, whereas genistein, indomethacin, probenecid and brefeldin A, which reverse multidrug-resistance-associated protein (MRP) function, exerted no effect.	Cyclosporine	83-96	ATP binding cassette subfamily C member 3	Homo sapiens	316-319