PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
22912749-1	2012	Cystinosis is a rare disease caused by homozygous mutations of the CTNS gene, encoding a cystine efflux channel in the lysosomal membrane.	Cystine	89-96	cystinosin, lysosomal cystine transporter	Homo sapiens	67-71	
22912749-3	2012	Here we show that human mesenchymal stem cells, from amniotic fluid or bone marrow, reduce pathologic cystine accumulation in co-cultured CTNS mutant fibroblasts or proximal tubular cells from cystinosis patients.	Cystine	102-109	cystinosin, lysosomal cystine transporter	Homo sapiens	138-142