PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26018082-1	2015	Leber congenital amaurosis 9 (LCA9) is an autosomal recessive retinal degeneration condition caused by mutations in the NAD(+) biosynthetic enzyme NMNAT1.	NAD	120-126	nicotinamide nucleotide adenylyltransferase 1	Homo sapiens	147-153