PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19403599-2	2009	A wide range of different hydrolysable and poorly hydrolysable nucleoside triphosphates were used to elucidate the role of ATP hydrolysis in CFTR function.	nucleoside triphosphates	63-87	CF transmembrane conductance regulator	Homo sapiens	141-145	
10581360-4	1999	Chloride channel activity of CFTR is dependent on protein phosphorylation and presence of nucleoside triphosphates.	nucleoside triphosphates	90-114	CF transmembrane conductance regulator	Homo sapiens	29-33	
12939393-3	2003	In hydrolyzable nucleoside triphosphates, PKA-phosphorylated CFTR channels open into bursts, lasting on the order of a second, from closed (interburst) intervals of a second or more.	nucleoside triphosphates	16-40	CF transmembrane conductance regulator	Homo sapiens	61-65	
12560093-1	2003	The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel which is activated by protein phosphorylation and nucleoside triphosphates.	nucleoside triphosphates	135-159	CF transmembrane conductance regulator	Homo sapiens	4-55	
12560093-1	2003	The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel which is activated by protein phosphorylation and nucleoside triphosphates.	nucleoside triphosphates	135-159	CF transmembrane conductance regulator	Homo sapiens	57-61	
14710196-3	2004	In addition, nucleoside triphosphates were shown to regulate the opening of phosphorylated CFTR.	nucleoside triphosphates	13-37	CF transmembrane conductance regulator	Homo sapiens	91-95	
7687826-1	1993	The cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel requires both phosphorylation of its R domain and the presence of nucleoside triphosphates for activation.	nucleoside triphosphates	141-165	CF transmembrane conductance regulator	Homo sapiens	4-55	
7520292-1	1994	Phosphorylated cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channels require nucleoside triphosphates, such as ATP, to open.	nucleoside triphosphates	95-119	CF transmembrane conductance regulator	Homo sapiens	15-66	
7520292-1	1994	Phosphorylated cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channels require nucleoside triphosphates, such as ATP, to open.	nucleoside triphosphates	95-119	CF transmembrane conductance regulator	Homo sapiens	68-72	
7687826-1	1993	The cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel requires both phosphorylation of its R domain and the presence of nucleoside triphosphates for activation.	nucleoside triphosphates	141-165	CF transmembrane conductance regulator	Homo sapiens	57-61	
7684867-1	1993	These results begin to indicate that nucleoside triphosphates directly regulate CFTR Cl- channels by interacting with the NBDs.	nucleoside triphosphates	37-61	CF transmembrane conductance regulator	Homo sapiens	80-84	
7522901-2	1993	CFTR contains two membrane-spanning domains (MSDs), two nucleotide-binding domains (NBDs), and a unique R domain; CFTR functions as a Cl- channel regulated by phosphorylation and by nucleoside triphosphates.	nucleoside triphosphates	182-206	CF transmembrane conductance regulator	Homo sapiens	0-4	
7522901-2	1993	CFTR contains two membrane-spanning domains (MSDs), two nucleotide-binding domains (NBDs), and a unique R domain; CFTR functions as a Cl- channel regulated by phosphorylation and by nucleoside triphosphates.	nucleoside triphosphates	182-206	CF transmembrane conductance regulator	Homo sapiens	114-118	
1718606-0	1991	Nucleoside triphosphates are required to open the CFTR chloride channel.	nucleoside triphosphates	0-24	CF transmembrane conductance regulator	Homo sapiens	50-54	
1718606-7	1991	The finding that nucleoside triphosphates regulate CFTR begins to explain why CF-associated mutations in the NBDs block Cl- channel function.	nucleoside triphosphates	17-41	CF transmembrane conductance regulator	Homo sapiens	51-55