PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
10220490-7	1999	From the known substrate specificities of UGT1A4 toward lamotrigine and bilirubin and our activity and inhibition data, we conclude that UGT1A4 is a major retigabine N-glucuronosyl transferase in vivo and significantly contributes to the enterohepatic cycling of the drug.	Lamotrigine	56-67	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	42-48	
10220490-7	1999	From the known substrate specificities of UGT1A4 toward lamotrigine and bilirubin and our activity and inhibition data, we conclude that UGT1A4 is a major retigabine N-glucuronosyl transferase in vivo and significantly contributes to the enterohepatic cycling of the drug.	Lamotrigine	56-67	UDP glucuronosyltransferase family 1 member A4	Homo sapiens	137-143