Willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures [clinicaltrials_resource:08dc0bccaf275d31678dd162f6a96d26]

Willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures [clinicaltrials_resource:08dc0bccaf275d31678dd162f6a96d26]

Inclusion Criteria [clinicaltrials_vocabulary:Inclusion-Criteria]
clinicaltrials resource [clinicaltrials_vocabulary:Resource]
http://bio2rdf.org/clinicaltrials_resource:08dc0bccaf275d31678dd162f6a96d26

Willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures [clinicaltrials_resource:08dc0bccaf275d31678dd162f6a96d26]

Inclusion Criteria [clinicaltrials_vocabulary:Inclusion-Criteria]
clinicaltrials resource [clinicaltrials_vocabulary:Resource]
http://bio2rdf.org/clinicaltrials_resource:08dc0bccaf275d31678dd162f6a96d26
Bio2RDF identifier
08dc0bccaf275d31678dd162f6a96d26
Bio2RDF namespace
Bio2RDF uri
http://bio2rdf.org/clinicaltrials_resource:08dc0bccaf275d31678dd162f6a96d26
identifier
clinicaltrials_resource:08dc0bccaf275d31678dd162f6a96d26
title
Willing and able to provide wr ...... ny research-related procedures
@en
inDataset
type
label
Willing and able to provide wr ...... c0bccaf275d31678dd162f6a96d26]
@en