PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24668066-1	2014	Conventional N-glycoproteome analysis usually applies C18 reversed-phase (RP) adsorbent for sample purification, which will lead to unavoidable sample loss due to the high hydrophilicity of N-glycopeptides.	n-glycopeptides	190-205	Bardet-Biedl syndrome 9	Homo sapiens	54-57	
24668066-3	2014	It was observed that the small hydrophilic N-glycopeptides that cannot retain onto C18 adsorbent can be captured by the graphitized carbon, while the large hydrophobic N-glycopeptides that cannot retain onto the graphitized carbon can be feasibly captured by the C18 adsorbent.	n-glycopeptides	43-58	Bardet-Biedl syndrome 9	Homo sapiens	83-86	
24668066-4	2014	Comparing with sample purification by using C18 adsorbent only, 28.5 % more N-glycopeptides were identified by combining both C18 and PGC adsorbents.	n-glycopeptides	76-91	Bardet-Biedl syndrome 9	Homo sapiens	44-47	
24668066-4	2014	Comparing with sample purification by using C18 adsorbent only, 28.5 % more N-glycopeptides were identified by combining both C18 and PGC adsorbents.	n-glycopeptides	76-91	Bardet-Biedl syndrome 9	Homo sapiens	126-129