signature of informed consent [clinicaltrials_resource:0b2c983ede4e7b3bc81d68cdd81d18b1]
eligibility for clinicaltrials:NCT01340235 [clinicaltrials_resource:0a0e81c08f307556ee1b05821dfae47d]eligibility for clinicaltrials:NCT02089802 [clinicaltrials_resource:3bc5cbd3757ece3a52cc33a4f5fa190f]eligibility for clinicaltrials:NCT01948115 [clinicaltrials_resource:816d05eb85279f64d9948c35dedd9a87]eligibility for clinicaltrials:NCT01968434 [clinicaltrials_resource:ef8aedc4c71e67281a87e3e596d5d925]eligibility for clinicaltrials:NCT00537511 [clinicaltrials_resource:f3cfa305b0ed95956ecd4c4b562183b5]
exclusion criteria [clinicaltrials_vocabulary:exclusion-criteria]
eligibility for clinicaltrials:NCT01340235 [clinicaltrials_resource:0a0e81c08f307556ee1b05821dfae47d]eligibility for clinicaltrials:NCT02089802 [clinicaltrials_resource:3bc5cbd3757ece3a52cc33a4f5fa190f]eligibility for clinicaltrials:NCT01948115 [clinicaltrials_resource:816d05eb85279f64d9948c35dedd9a87]eligibility for clinicaltrials:NCT01968434 [clinicaltrials_resource:ef8aedc4c71e67281a87e3e596d5d925]eligibility for clinicaltrials:NCT00537511 [clinicaltrials_resource:f3cfa305b0ed95956ecd4c4b562183b5]
inclusion criteria [clinicaltrials_vocabulary:inclusion-criteria]
signature of informed consent [clinicaltrials_resource:0b2c983ede4e7b3bc81d68cdd81d18b1]
Bio2RDF identifier
0b2c983ede4e7b3bc81d68cdd81d18b1
Bio2RDF namespace
clinicaltrials_resource
Bio2RDF uri
http://bio2rdf.org/clinicaltrials_resource:0b2c983ede4e7b3bc81d68cdd81d18b1
identifier
clinicaltrials_resource:0b2c983ede4e7b3bc81d68cdd81d18b1
title
signature of informed consent
@en
type
label
signature of informed consent [clinicaltrials_resource:0b2c983ede4e7b3bc81d68cdd81d18b1]
@en