PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25123131-0	2014	A combination of eicosapentaenoic acid-free fatty acid, epigallocatechin-3-gallate and proanthocyanidins has a strong effect on mTOR signaling in colorectal cancer cells.	Fatty Acids, Nonesterified	39-54	mechanistic target of rapamycin kinase	Homo sapiens	128-132	
32640259-5	2020	RHOA mutations in cancer cells activated the PI3K-AKT-mTOR signaling pathway, increasing production of free fatty acids that are more effectively consumed by Treg cells than effector T cells.	Fatty Acids, Nonesterified	103-119	mechanistic target of rapamycin kinase	Homo sapiens	54-58	
30862719-0	2019	Free Fatty Acids Rewire Cancer Metabolism in Obesity-Associated Breast Cancer via Estrogen Receptor and mTOR Signaling.	Fatty Acids, Nonesterified	0-16	mechanistic target of rapamycin kinase	Homo sapiens	104-108	
12837665-1	2003	The purpose of the study described herein was to investigate how the mammalian target of rapamycin (mTOR)-signaling pathway and eukaryotic initiation factor 2B (eIF2B) activity, both having key roles in the translational control of protein synthesis in skeletal muscle, are regulated in cardiac muscle of rats in response to two different models of altered free fatty acid (FFA) and insulin availability.	Fatty Acids, Nonesterified	357-372	mechanistic target of rapamycin kinase	Homo sapiens	69-98	
12837665-1	2003	The purpose of the study described herein was to investigate how the mammalian target of rapamycin (mTOR)-signaling pathway and eukaryotic initiation factor 2B (eIF2B) activity, both having key roles in the translational control of protein synthesis in skeletal muscle, are regulated in cardiac muscle of rats in response to two different models of altered free fatty acid (FFA) and insulin availability.	Fatty Acids, Nonesterified	357-372	mechanistic target of rapamycin kinase	Homo sapiens	100-104	
12837665-1	2003	The purpose of the study described herein was to investigate how the mammalian target of rapamycin (mTOR)-signaling pathway and eukaryotic initiation factor 2B (eIF2B) activity, both having key roles in the translational control of protein synthesis in skeletal muscle, are regulated in cardiac muscle of rats in response to two different models of altered free fatty acid (FFA) and insulin availability.	Fatty Acids, Nonesterified	374-377	mechanistic target of rapamycin kinase	Homo sapiens	69-98	
12837665-1	2003	The purpose of the study described herein was to investigate how the mammalian target of rapamycin (mTOR)-signaling pathway and eukaryotic initiation factor 2B (eIF2B) activity, both having key roles in the translational control of protein synthesis in skeletal muscle, are regulated in cardiac muscle of rats in response to two different models of altered free fatty acid (FFA) and insulin availability.	Fatty Acids, Nonesterified	374-377	mechanistic target of rapamycin kinase	Homo sapiens	100-104