PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
20301289-0	1993	PMM2-CDG (CDG-Ia) CLINICAL CHARACTERISTICS: PMM2-CDG (CDG-Ia) (previously known as congenital disorder of glycosylation type 1a), the most common of a group of disorders of abnormal glycosylation of N-linked oligosaccharides, is divided into three types: infantile multisystem, late-infantile and childhood ataxia-intellectual disability, and adult stable disability.	n-linked oligosaccharides	199-224	phosphomannomutase 2	Homo sapiens	0-4	
20301289-0	1993	PMM2-CDG (CDG-Ia) CLINICAL CHARACTERISTICS: PMM2-CDG (CDG-Ia) (previously known as congenital disorder of glycosylation type 1a), the most common of a group of disorders of abnormal glycosylation of N-linked oligosaccharides, is divided into three types: infantile multisystem, late-infantile and childhood ataxia-intellectual disability, and adult stable disability.	n-linked oligosaccharides	199-224	phosphomannomutase 2	Homo sapiens	44-48