PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24098344-6	2013	Following DOX however, CK-M-OE hearts had better preservation of creatine phosphate and higher CK flux and higher EF as compared to control DOX hearts.	Phosphocreatine	65-83	creatine kinase, muscle	Mus musculus	23-27	
9746466-2	1998	Phosphocreatine (PCr) and ATP concentrations in M-CK-deficient hearts were not significantly different from those in wild-type hearts.	Phosphocreatine	0-15	creatine kinase, muscle	Mus musculus	48-52	
32372868-8	2020	The direct binding activated CK-MM activity in vitro and in vivo, which increased the levels of tissue phosphocreatine and strengthened the function of the creatine kinase/phosphocreatine system in skeletal muscle, thus buffering cellular ATP, delaying exercise-induced lactate accumulation, and improving exercise performance in mice.	Phosphocreatine	103-118	creatine kinase, muscle	Mus musculus	29-34	
32372868-8	2020	The direct binding activated CK-MM activity in vitro and in vivo, which increased the levels of tissue phosphocreatine and strengthened the function of the creatine kinase/phosphocreatine system in skeletal muscle, thus buffering cellular ATP, delaying exercise-induced lactate accumulation, and improving exercise performance in mice.	Phosphocreatine	172-187	creatine kinase, muscle	Mus musculus	29-34	
24098344-6	2013	Following DOX however, CK-M-OE hearts had better preservation of creatine phosphate and higher CK flux and higher EF as compared to control DOX hearts.	Phosphocreatine	65-83	creatine kinase, muscle	Mus musculus	23-25