PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31093697-3	2019	Modification of a self-signal trigging CD47-peptide on the NPs" surface decreased internalization by 10 times, (2.79 +- 0.21) x 104 Ru(bpy)3@SiO2-COOH and (0.28 +- 0.04) x 104 Ru(bpy)3@SiO2@CD47-peptide NPs per RAW264.7 macrophage (n = 5).	Silicon Dioxide	141-145	CD47 molecule	Homo sapiens	39-43	
31093697-3	2019	Modification of a self-signal trigging CD47-peptide on the NPs" surface decreased internalization by 10 times, (2.79 +- 0.21) x 104 Ru(bpy)3@SiO2-COOH and (0.28 +- 0.04) x 104 Ru(bpy)3@SiO2@CD47-peptide NPs per RAW264.7 macrophage (n = 5).	Silicon Dioxide	141-145	CD47 molecule	Homo sapiens	190-194	
31093697-3	2019	Modification of a self-signal trigging CD47-peptide on the NPs" surface decreased internalization by 10 times, (2.79 +- 0.21) x 104 Ru(bpy)3@SiO2-COOH and (0.28 +- 0.04) x 104 Ru(bpy)3@SiO2@CD47-peptide NPs per RAW264.7 macrophage (n = 5).	Silicon Dioxide	185-189	CD47 molecule	Homo sapiens	39-43	
31093697-5	2019	Furthermore, the interaction between CD47-peptide and SIRPalpha as well as the changes of the remaining free SIRPalpha during the internalization process of Ru(bpy)3@SiO2@CD47-peptide NPs were quantitatively evaluated, providing direct experimental evidence of the longspeculated crucial CD47-SIRPalpha interaction for drug-nanocarriers to escape internalization by phagocytic cells.	Silicon Dioxide	166-170	CD47 molecule	Homo sapiens	37-41	
31093697-5	2019	Furthermore, the interaction between CD47-peptide and SIRPalpha as well as the changes of the remaining free SIRPalpha during the internalization process of Ru(bpy)3@SiO2@CD47-peptide NPs were quantitatively evaluated, providing direct experimental evidence of the longspeculated crucial CD47-SIRPalpha interaction for drug-nanocarriers to escape internalization by phagocytic cells.	Silicon Dioxide	166-170	CD47 molecule	Homo sapiens	171-175	
31093697-5	2019	Furthermore, the interaction between CD47-peptide and SIRPalpha as well as the changes of the remaining free SIRPalpha during the internalization process of Ru(bpy)3@SiO2@CD47-peptide NPs were quantitatively evaluated, providing direct experimental evidence of the longspeculated crucial CD47-SIRPalpha interaction for drug-nanocarriers to escape internalization by phagocytic cells.	Silicon Dioxide	166-170	CD47 molecule	Homo sapiens	171-175