PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
33836297-3	2021	This ferrate dosage effect was diminished greatly in the condition of excess PMSO where ferrate self-decomposition was lessened largely, or counterbalanced by adding a strong complexing ligand (e.g. pyrophosphate) to sequester Fe(V) oxidation, demonstrating that the Fe(V) species derived from ferrate self-decomposition plays an important role in PMSO oxidation.	pmso	77-81	FEV transcription factor, ETS family member	Homo sapiens	227-232	
33836297-3	2021	This ferrate dosage effect was diminished greatly in the condition of excess PMSO where ferrate self-decomposition was lessened largely, or counterbalanced by adding a strong complexing ligand (e.g. pyrophosphate) to sequester Fe(V) oxidation, demonstrating that the Fe(V) species derived from ferrate self-decomposition plays an important role in PMSO oxidation.	pmso	77-81	FEV transcription factor, ETS family member	Homo sapiens	267-272	
33836297-4	2021	A mechanistic kinetics model involving the ferrate self-decomposition and PMSO oxidation by Fe(VI), Fe(V) and Fe(IV) species was then developed and validated.	pmso	74-78	FEV transcription factor, ETS family member	Homo sapiens	100-105	
33836297-5	2021	The modeling results show that up to 99% of the PMSO oxidation was contributed by the ferrate self-decomposition resultant Fe(V) species in borate buffer, revealing that ferrate self-decomposition is also a self-activation process.	pmso	48-52	FEV transcription factor, ETS family member	Homo sapiens	123-128	
30897545-8	2019	High-valent metal-oxo intermediates Fe(V)/Fe(IV) formed in situ from the reaction of CNT with Fe(VI) were likely responsible for this activation effect of CNT, which was further confirmed via using methyl phenyl sulfoxide (PMSO) as a probe compound.	pmso	223-227	FEV transcription factor, ETS family member	Homo sapiens	36-41