PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26861753-4	2016	OCT1 downregulation by shRNA impaired daunorubicin uptake into the TOV2223G cells, and these cells were significantly more resistant to the drug in comparison to the control shRNA.	Daunorubicin	38-50	solute carrier family 22 member 1	Homo sapiens	0-4	
26861753-0	2016	The human organic cation transporter OCT1 mediates high affinity uptake of the anticancer drug daunorubicin.	Daunorubicin	95-107	solute carrier family 22 member 1	Homo sapiens	37-41	
26861753-3	2016	Using the high-grade serous ovarian cancer cell line TOV2223G, we show that OCT1 mediated the high affinity (Km ~ 5 muM) uptake of daunorubicin into the cells, and that micromolar amounts of choline completely abolished the drug entry.	Daunorubicin	131-143	solute carrier family 22 member 1	Homo sapiens	76-80