PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
11478590-0	2001	Thiocyanate as a probe of the cystic fibrosis transmembrane conductance regulator chloride channel pore.	thiocyanate	0-11	CF transmembrane conductance regulator	Homo sapiens	30-81	
19918082-4	2009	Although commonly known as a Cl(-) channel, CFTR also conducts thiocyanate (SCN(-)) ions, important because, in several ways, they can limit potentially harmful accumulations of hydrogen peroxide (H(2)O(2)) and hypochlorite (OCl(-)).	thiocyanate	63-74	CF transmembrane conductance regulator	Homo sapiens	44-48	
16934416-8	2007	Additionally, this new model of cystic fibrosis pathology, clarifies the relationship between the CFTR and the multi-drug resistance proteins, and the lack of cell-mediated immunity by predicting that the substrate of these proteins is a glutathione adduct of thiocyanate.	thiocyanate	260-271	CF transmembrane conductance regulator	Homo sapiens	98-102	
34831067-7	2021	Yet, the CFTR protein also regulates numerous other pathways, such as the transport of HCO3-, glutathione and thiocyanate, immune cells, and the metabolism of lipids.	thiocyanate	110-121	CF transmembrane conductance regulator	Homo sapiens	9-13	
31027466-3	2019	CFTR, an adenosine triphosphate binding anion channel, has multiple functions, but primarily regulates the movement of chloride anions, thiocyanate and bicarbonate across luminal cell membranes.	thiocyanate	136-147	CF transmembrane conductance regulator	Homo sapiens	0-4