PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
29934308-4	2018	Here, we report the heterodimeric structure of FXR and RXR in the presence of an FXR agonist (WAY-362450), RXR agonist (9-cis-retinoic acid), and a peptide derived from a steroid receptor coactivator (SRC2), revealing both unique and conserved modes for FXR heterodimerization.	Alitretinoin	120-139	nuclear receptor subfamily 1 group H member 4	Homo sapiens	47-50	
16037943-7	2005	In these cells, the FXR pharmacological agonist GW4064 upregulated VPAC1 expression in a dose-dependent manner, and this effect was antagonized by the RXRalpha ligand, 9-cis retinoic acid.	Alitretinoin	168-187	nuclear receptor subfamily 1 group H member 4	Homo sapiens	20-23	
24498423-2	2014	FXR is activated by bile acids, RXRalpha by the vitamin A-derivative 9-cis retinoic acid (9cRA).	Alitretinoin	69-88	nuclear receptor subfamily 1 group H member 4	Homo sapiens	0-3	
24498423-2	2014	FXR is activated by bile acids, RXRalpha by the vitamin A-derivative 9-cis retinoic acid (9cRA).	Alitretinoin	90-94	nuclear receptor subfamily 1 group H member 4	Homo sapiens	0-3