PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
33573095-3	2021	Severity of indomethacin-induced enteropathy in FcgRIIb-/- mice was higher than WT mice as demonstrated by survival analysis, intestinal injury (histology, immune-deposition, and intestinal cytokines), gut leakage (FITC-dextran assay and endotoxemia), serum cytokines, and lupus characteristics (anti-dsDNA, renal injury, and proteinuria).	Indomethacin	12-24	Fc receptor, IgG, low affinity IIb	Mus musculus	48-55	
33573095-6	2021	In conclusion, gut leakage-induced endotoxemia is more severe in indomethacin-administered FcgRIIb-/- mice than WT, possibly due to the enhanced indomethacin toxicity from lupus-induced intestinal immune-deposition.	Indomethacin	65-77	Fc receptor, IgG, low affinity IIb	Mus musculus	91-98	
33573095-6	2021	In conclusion, gut leakage-induced endotoxemia is more severe in indomethacin-administered FcgRIIb-/- mice than WT, possibly due to the enhanced indomethacin toxicity from lupus-induced intestinal immune-deposition.	Indomethacin	145-157	Fc receptor, IgG, low affinity IIb	Mus musculus	91-98