PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
28402605-0	2017	Biotin-thiamine responsive basal ganglia disease: Identification of a pyruvate peak on brain spectroscopy, novel mutation in SLC19A3, and calculation of prevalence based on allele frequencies from aggregated next-generation sequencing data.	Thiamine	7-15	solute carrier family 19 member 3	Homo sapiens	125-132	
28402605-1	2017	Biotin-thiamine responsive basal ganglia disease is an inborn error of metabolism caused by mutations in SLC19A3, encoding a transporter of thiamine across the plasma membrane.	Thiamine	7-15	solute carrier family 19 member 3	Homo sapiens	105-112	
28402605-1	2017	Biotin-thiamine responsive basal ganglia disease is an inborn error of metabolism caused by mutations in SLC19A3, encoding a transporter of thiamine across the plasma membrane.	Thiamine	140-148	solute carrier family 19 member 3	Homo sapiens	105-112