PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31061755-0	2019	Biotin-Thiamine Responsive Encephalopathy: Report of an Egyptian Family with a Novel SLC19A3 Mutation and Review of the Literature.	Biotin	0-6	solute carrier family 19 member 3	Homo sapiens	85-92	
31061755-1	2019	Biotin-thiamine responsive basal ganglia disease (BTRBGD) is an autosomal recessive neurometabolic disorder with poor genotype-phenotype correlation, caused by mutations in the SLC19A3 gene on chromosome 2q36.6.	Biotin	0-6	solute carrier family 19 member 3	Homo sapiens	177-184