PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16805961-4	2006	Because both drugs are transported via P-glycoprotein and breast cancer resistance protein and metabolized by cytochrome P450 3A2, the interaction of imatinib mesilate with these proteins may be responsible for the increased intestinal absorption of ciclosporin in rats.	Imatinib Mesylate	150-158	ATP-binding cassette, subfamily B (MDR/TAP), member 1B	Rattus norvegicus	39-53