PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
30651282-1	2019	Mutations in NCF1 (p47phox) cause autosomal recessive chronic granulomatous disease (CGD) with abnormal dihydrorhodamine (DHR) assay and absent p47phox protein.	dhr	122-125	neutrophil cytosolic factor 1	Homo sapiens	13-17	
30651282-1	2019	Mutations in NCF1 (p47phox) cause autosomal recessive chronic granulomatous disease (CGD) with abnormal dihydrorhodamine (DHR) assay and absent p47phox protein.	dhr	122-125	neutrophil cytosolic factor 1	Homo sapiens	19-26