PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
30354245-1	2018	Objective- Palmitoylethanolamide is an endogenous fatty acid mediator that is synthetized from membrane phospholipids by N-acyl phosphatidylethanolamine phospholipase D. Its biological actions are primarily mediated by PPAR-alpha (peroxisome proliferator-activated receptors alpha) and the orphan receptor GPR55.	palmidrol	11-32	peroxisome proliferator activated receptor alpha	Mus musculus	219-229	
30354245-1	2018	Objective- Palmitoylethanolamide is an endogenous fatty acid mediator that is synthetized from membrane phospholipids by N-acyl phosphatidylethanolamine phospholipase D. Its biological actions are primarily mediated by PPAR-alpha (peroxisome proliferator-activated receptors alpha) and the orphan receptor GPR55.	palmidrol	11-32	G protein-coupled receptor 55	Mus musculus	306-311	
30354245-1	2018	Objective- Palmitoylethanolamide is an endogenous fatty acid mediator that is synthetized from membrane phospholipids by N-acyl phosphatidylethanolamine phospholipase D. Its biological actions are primarily mediated by PPAR-alpha (peroxisome proliferator-activated receptors alpha) and the orphan receptor GPR55.	Fatty Acids	50-60	peroxisome proliferator activated receptor alpha	Mus musculus	219-229	
30354245-1	2018	Objective- Palmitoylethanolamide is an endogenous fatty acid mediator that is synthetized from membrane phospholipids by N-acyl phosphatidylethanolamine phospholipase D. Its biological actions are primarily mediated by PPAR-alpha (peroxisome proliferator-activated receptors alpha) and the orphan receptor GPR55.	Fatty Acids	50-60	G protein-coupled receptor 55	Mus musculus	306-311	
30354245-1	2018	Objective- Palmitoylethanolamide is an endogenous fatty acid mediator that is synthetized from membrane phospholipids by N-acyl phosphatidylethanolamine phospholipase D. Its biological actions are primarily mediated by PPAR-alpha (peroxisome proliferator-activated receptors alpha) and the orphan receptor GPR55.	Phospholipids	104-117	peroxisome proliferator activated receptor alpha	Mus musculus	219-229	
30354245-1	2018	Objective- Palmitoylethanolamide is an endogenous fatty acid mediator that is synthetized from membrane phospholipids by N-acyl phosphatidylethanolamine phospholipase D. Its biological actions are primarily mediated by PPAR-alpha (peroxisome proliferator-activated receptors alpha) and the orphan receptor GPR55.	Phospholipids	104-117	G protein-coupled receptor 55	Mus musculus	306-311	
30354245-8	2018	Mechanistically, we found that palmitoylethanolamide, by activating GPR55, increases the expression of the phagocytosis receptor MerTK (proto-oncogene tyrosine-protein kinase MER) and enhances macrophage efferocytosis, indicative of proresolving properties.	palmidrol	31-52	G protein-coupled receptor 55	Mus musculus	68-73	
30354245-8	2018	Mechanistically, we found that palmitoylethanolamide, by activating GPR55, increases the expression of the phagocytosis receptor MerTK (proto-oncogene tyrosine-protein kinase MER) and enhances macrophage efferocytosis, indicative of proresolving properties.	palmidrol	31-52	MER proto-oncogene tyrosine kinase	Mus musculus	129-134