All patients must sign informed consent approved by the Committee on the Use of Human Subjects at the University of Minnesota [clinicaltrials_resource:db3bda6074dcad07b3d8125a45c8922f]

All patients must sign informed consent approved by the Committee on the Use of Human Subjects at the University of Minnesota [clinicaltrials_resource:db3bda6074dcad07b3d8125a45c8922f]

Inclusion Criteria [clinicaltrials_vocabulary:Inclusion-Criteria]
clinicaltrials resource [clinicaltrials_vocabulary:Resource]
http://bio2rdf.org/clinicaltrials_resource:db3bda6074dcad07b3d8125a45c8922f

All patients must sign informed consent approved by the Committee on the Use of Human Subjects at the University of Minnesota [clinicaltrials_resource:db3bda6074dcad07b3d8125a45c8922f]

Inclusion Criteria [clinicaltrials_vocabulary:Inclusion-Criteria]
clinicaltrials resource [clinicaltrials_vocabulary:Resource]
http://bio2rdf.org/clinicaltrials_resource:db3bda6074dcad07b3d8125a45c8922f
Bio2RDF identifier
db3bda6074dcad07b3d8125a45c8922f
Bio2RDF namespace
Bio2RDF uri
http://bio2rdf.org/clinicaltrials_resource:db3bda6074dcad07b3d8125a45c8922f
identifier
clinicaltrials_resource:db3bda6074dcad07b3d8125a45c8922f
title
All patients must sign informe ...... at the University of Minnesota
@en
inDataset
type
label
All patients must sign informe ...... bda6074dcad07b3d8125a45c8922f]
@en