PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16730994-4	2006	The second inhibitor molecule binds with the carboxyl group at the pyrimidine recognition site and the uridine moiety exploits interactions with RNase A residues Lys66, His119 and Asp121.	Uridine	103-110	ribonuclease A family member 1, pancreatic	Homo sapiens	145-152	
22006382-11	2011	Initial observations confirm that RNase A type degradation with strand cleavage on the 3" side of uridine or cytosine is the dominant cleavage pattern in serum.	Uridine	98-105	ribonuclease A family member 1, pancreatic	Homo sapiens	34-41	
11456753-1	2001	Two synthetically modified nucleoside triphosphate analogues (adenosine modified with an imidazole and uridine modified with a cationic amine) are enzymatically polymerized in tandem along a degenerate DNA library for the combinatorial selection of an RNAse A mimic.	Uridine	103-110	ribonuclease A family member 1, pancreatic	Homo sapiens	252-259	
34695708-5	2021	Our investigations revealed that uridine conjugates were quickly cleaved by RNase A, releasing silybin drugs, even at low enzyme concentrations.	Uridine	33-40	ribonuclease A family member 1, pancreatic	Homo sapiens	76-83