NCT00058266 arm group 0bb4dda796362c0d7a33b81c9291567d [clinicaltrials_resource:NCT00058266/arm-group/0bb4dda796362c0d7a33b81c9291567d]
arm group [clinicaltrials_vocabulary:arm-group]
NCT00058266 arm group 0bb4dda796362c0d7a33b81c9291567d [clinicaltrials_resource:NCT00058266/arm-group/0bb4dda796362c0d7a33b81c9291567d]
Bio2RDF identifier
NCT00058266/arm-group/0bb4dda796362c0d7a33b81c9291567d
Bio2RDF namespace
clinicaltrials_resource
Bio2RDF uri
http://bio2rdf.org/clinicaltri ...... b4dda796362c0d7a33b81c9291567d
description [clinicaltrials_vocabulary:description]
Patients undergo radical prost ...... tein as in arm I for 3 months.
identifier
clinicaltrials_resource:NCT00058266/arm-group/0bb4dda796362c0d7a33b81c9291567d
title
NCT00058266 arm group 0bb4dda796362c0d7a33b81c9291567d
@en
type
label
NCT00058266 arm group 0bb4dda7 ...... 4dda796362c0d7a33b81c9291567d]
@en