PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27288078-0	2016	Choline on the Move: Perspectives on the Molecular Physiology and Pharmacology of the Presynaptic Choline Transporter.	Choline	0-7	solute carrier family 5 member 7	Homo sapiens	98-117	
27288078-2	2016	High-affinity choline uptake (HACU) was one of the last features of cholinergic signaling to be defined at a molecular level, achieved through the cloning of the choline transporter (CHT, SLC5A7).	Choline	14-21	solute carrier family 5 member 7	Homo sapiens	162-181	
27288078-2	2016	High-affinity choline uptake (HACU) was one of the last features of cholinergic signaling to be defined at a molecular level, achieved through the cloning of the choline transporter (CHT, SLC5A7).	Choline	14-21	solute carrier family 5 member 7	Homo sapiens	183-186	
27288078-2	2016	High-affinity choline uptake (HACU) was one of the last features of cholinergic signaling to be defined at a molecular level, achieved through the cloning of the choline transporter (CHT, SLC5A7).	Choline	14-21	solute carrier family 5 member 7	Homo sapiens	188-194	
27288078-3	2016	In retrospect, the molecular era of CHT studies initiated with the identification of hemicholinium-3 (HC-3), a potent, competitive CHT antagonist, though it would take another 30 years before HC-3, in radiolabeled form, was used by Joseph Coyle"s laboratory to identify and monitor the dynamics of CHT proteins.	Hemicholinium 3	85-100	solute carrier family 5 member 7	Homo sapiens	36-39	
27288078-3	2016	In retrospect, the molecular era of CHT studies initiated with the identification of hemicholinium-3 (HC-3), a potent, competitive CHT antagonist, though it would take another 30 years before HC-3, in radiolabeled form, was used by Joseph Coyle"s laboratory to identify and monitor the dynamics of CHT proteins.	Hemicholinium 3	85-100	solute carrier family 5 member 7	Homo sapiens	131-134	
27288078-3	2016	In retrospect, the molecular era of CHT studies initiated with the identification of hemicholinium-3 (HC-3), a potent, competitive CHT antagonist, though it would take another 30 years before HC-3, in radiolabeled form, was used by Joseph Coyle"s laboratory to identify and monitor the dynamics of CHT proteins.	Hemicholinium 3	85-100	solute carrier family 5 member 7	Homo sapiens	131-134	
27288078-3	2016	In retrospect, the molecular era of CHT studies initiated with the identification of hemicholinium-3 (HC-3), a potent, competitive CHT antagonist, though it would take another 30 years before HC-3, in radiolabeled form, was used by Joseph Coyle"s laboratory to identify and monitor the dynamics of CHT proteins.	Hydrocortisone	102-104	solute carrier family 5 member 7	Homo sapiens	36-39	
27288078-3	2016	In retrospect, the molecular era of CHT studies initiated with the identification of hemicholinium-3 (HC-3), a potent, competitive CHT antagonist, though it would take another 30 years before HC-3, in radiolabeled form, was used by Joseph Coyle"s laboratory to identify and monitor the dynamics of CHT proteins.	Hydrocortisone	102-104	solute carrier family 5 member 7	Homo sapiens	131-134	
27288078-3	2016	In retrospect, the molecular era of CHT studies initiated with the identification of hemicholinium-3 (HC-3), a potent, competitive CHT antagonist, though it would take another 30 years before HC-3, in radiolabeled form, was used by Joseph Coyle"s laboratory to identify and monitor the dynamics of CHT proteins.	Hydrocortisone	102-104	solute carrier family 5 member 7	Homo sapiens	131-134