PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
7588324-1	1995	The 1,25-dihydroxyvitamin D3 (vitamin D) receptor (VDR) is a key trans-activating protein that mediates calcium regulation as well as cellular proliferation and differentiation.	Calcium	104-111	vitamin D receptor	Rattus norvegicus	30-49	
7588324-1	1995	The 1,25-dihydroxyvitamin D3 (vitamin D) receptor (VDR) is a key trans-activating protein that mediates calcium regulation as well as cellular proliferation and differentiation.	Calcium	104-111	vitamin D receptor	Rattus norvegicus	51-54	
7588324-5	1995	Vitamin D-induced transcription was assayed in transfected ROS 17/2.8 osteosarcoma cells using chloraminphenicol acetyltransferase constructs containing the vitamin D-responsive element (VDRE) at its native locus in the rat OC promoter as well as fused to a heterologous promoter.	Vitamin D	0-9	bone gamma-carboxyglutamate protein	Rattus norvegicus	224-226	
7588324-6	1995	Both ST and OA inhibit VDRE-mediated and vitamin D-dependent enhancement of OC gene transcription as well as OC biosynthesis, as assessed by RIAs.	Vitamin D	41-50	bone gamma-carboxyglutamate protein	Rattus norvegicus	76-78	
7588324-8	1995	In contrast, OA does inhibit the formation of complexes interacting with both the OC and osteopontin VDREs; immunoprecipitation studies using 32P-labeled ROS 17/2.8 cells reveal that OA treatment result in ligand-independent hyperphosphorylation of the VDR.	Phosphorus-32	142-145	bone gamma-carboxyglutamate protein	Rattus norvegicus	82-84	
7588324-8	1995	In contrast, OA does inhibit the formation of complexes interacting with both the OC and osteopontin VDREs; immunoprecipitation studies using 32P-labeled ROS 17/2.8 cells reveal that OA treatment result in ligand-independent hyperphosphorylation of the VDR.	Phosphorus-32	142-145	vitamin D receptor	Rattus norvegicus	101-104	
7588324-8	1995	In contrast, OA does inhibit the formation of complexes interacting with both the OC and osteopontin VDREs; immunoprecipitation studies using 32P-labeled ROS 17/2.8 cells reveal that OA treatment result in ligand-independent hyperphosphorylation of the VDR.	ros	154-157	vitamin D receptor	Rattus norvegicus	101-104