PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27785023-5	2016	A series of studies on the action mechanism showed that the polymer components such as beta-cyclodextrin, hydrophobic poly(d,l-lactide) segment, and poly(ethylene glycol) coordinatively contributed to the improved intracellular ATP depletion and ATPase activity, increased intracellular uptake of P-gp substrates via competitive binding to P-gp, and decreased P-gp expression in MCF-7/ADR cells.	betadex	87-104	ATP binding cassette subfamily B member 1	Homo sapiens	297-301	
27785023-5	2016	A series of studies on the action mechanism showed that the polymer components such as beta-cyclodextrin, hydrophobic poly(d,l-lactide) segment, and poly(ethylene glycol) coordinatively contributed to the improved intracellular ATP depletion and ATPase activity, increased intracellular uptake of P-gp substrates via competitive binding to P-gp, and decreased P-gp expression in MCF-7/ADR cells.	betadex	87-104	ATP binding cassette subfamily B member 1	Homo sapiens	340-344	
27785023-5	2016	A series of studies on the action mechanism showed that the polymer components such as beta-cyclodextrin, hydrophobic poly(d,l-lactide) segment, and poly(ethylene glycol) coordinatively contributed to the improved intracellular ATP depletion and ATPase activity, increased intracellular uptake of P-gp substrates via competitive binding to P-gp, and decreased P-gp expression in MCF-7/ADR cells.	betadex	87-104	ATP binding cassette subfamily B member 1	Homo sapiens	340-344