PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9535788-1	1998	Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS).	Methyl Methanesulfonate	193-216	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	60-74	
9535788-1	1998	Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS).	Methyl Methanesulfonate	193-216	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	76-80	
9535788-1	1998	Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS).	Methyl Methanesulfonate	218-221	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	60-74	
9535788-1	1998	Expression of multidrug resistance (mdr) genes encoding the P-glycoprotein (P-gp) drug efflux pump was analysed in cultured rat liver epithelial cells acutely treated by the DNA-damaging agent methyl methanesulfonate (MMS).	Methyl Methanesulfonate	218-221	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	76-80	
9535788-4	1998	In addition, the DNA-damaging agent was found to enhance in a dose-dependent manner cellular efflux of the P-gp substrate rhodamine 123, which was inhibited by the P-gp inhibitor verapamil, thus providing evidence that exposure to MMS led to increased P-gp-related drug transport in rat liver cells.	Methyl Methanesulfonate	231-234	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	107-111	
9535788-4	1998	In addition, the DNA-damaging agent was found to enhance in a dose-dependent manner cellular efflux of the P-gp substrate rhodamine 123, which was inhibited by the P-gp inhibitor verapamil, thus providing evidence that exposure to MMS led to increased P-gp-related drug transport in rat liver cells.	Methyl Methanesulfonate	231-234	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	164-168	
9535788-4	1998	In addition, the DNA-damaging agent was found to enhance in a dose-dependent manner cellular efflux of the P-gp substrate rhodamine 123, which was inhibited by the P-gp inhibitor verapamil, thus providing evidence that exposure to MMS led to increased P-gp-related drug transport in rat liver cells.	Methyl Methanesulfonate	231-234	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	164-168