PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23095029-9	2013	Hence, the data on new LTA(4)H inhibitors should be cautiously interpreted with regard to potential repercussions of preventing PGP degradation as well as for the clinical benefits of concomitant lipoxin formation.	Lipoxins	196-203	leukotriene A4 hydrolase	Homo sapiens	23-30	
27643598-2	2016	Leukotriene A4 hydroxylase (LTA4H), an enzyme which converts LTA4 to LTB4, regulates the balance between the anti-inflammatory lipoxins and pro-inflammatory LTB4, with direct implications in TB-driven inflammation.	Lipoxins	127-135	leukotriene A4 hydrolase	Homo sapiens	0-26	
27643598-2	2016	Leukotriene A4 hydroxylase (LTA4H), an enzyme which converts LTA4 to LTB4, regulates the balance between the anti-inflammatory lipoxins and pro-inflammatory LTB4, with direct implications in TB-driven inflammation.	Lipoxins	127-135	leukotriene A4 hydrolase	Homo sapiens	28-33	
22304914-3	2012	Modulation of the leukotriene A(4) hydrolase (LTA4H) locus, which controls the balance of pro- and anti-inflammatory eicosanoids, reveals two distinct molecular routes to mycobacterial susceptibility converging on dysregulated TNF levels: inadequate inflammation caused by excess lipoxins and hyperinflammation driven by excess leukotriene B(4).	Lipoxins	280-288	leukotriene A4 hydrolase	Homo sapiens	18-44	
20211140-4	2010	lta4h mutations confer hypersusceptibility independent of LTB(4) reduction, by redirecting eicosanoid substrates to anti-inflammatory lipoxins.	Lipoxins	134-142	leukotriene A4 hydrolase	Homo sapiens	0-5	
22304914-3	2012	Modulation of the leukotriene A(4) hydrolase (LTA4H) locus, which controls the balance of pro- and anti-inflammatory eicosanoids, reveals two distinct molecular routes to mycobacterial susceptibility converging on dysregulated TNF levels: inadequate inflammation caused by excess lipoxins and hyperinflammation driven by excess leukotriene B(4).	Lipoxins	280-288	leukotriene A4 hydrolase	Homo sapiens	46-51