PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24189249-2	2014	An in situ single-pass intestinal perfusion study in rats with the P-gp inhibitor verapamil or quinidine and an ATPase assay with human P-gp membranes indicated that lumefantrine is a substrate of P-gp which limits its intestinal absorption.	Lumefantrine	166-178	phosphoglycolate phosphatase	Homo sapiens	136-140	
24189249-2	2014	An in situ single-pass intestinal perfusion study in rats with the P-gp inhibitor verapamil or quinidine and an ATPase assay with human P-gp membranes indicated that lumefantrine is a substrate of P-gp which limits its intestinal absorption.	Lumefantrine	166-178	phosphoglycolate phosphatase	Homo sapiens	136-140