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7737253
Source:
http://linkedlifedata.com/resource/pubmed/id/7737253
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(
52
)
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0008976
,
umls-concept:C0013331
,
umls-concept:C0030705
,
umls-concept:C0034656
,
umls-concept:C0036043
,
umls-concept:C0149473
,
umls-concept:C0205179
,
umls-concept:C0205390
,
umls-concept:C0332177
,
umls-concept:C0376358
,
umls-concept:C0679729
,
umls-concept:C1257890
,
umls-concept:C1707877
,
umls-concept:C1710133
pubmed:dateCreated
1995-6-8
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/7512719
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Delayed-Action Preparations
,
http://linkedlifedata.com/resource/pubmed/chemical/Goserelin
pubmed:status
MEDLINE
pubmed:issn
0302-2838
pubmed:author
pubmed-author:DebruyneF MFM
,
pubmed-author:DijkmanG AGA
,
pubmed-author:Fernandez del MoralPP
,
pubmed-author:HoefakkerJ WJW
,
pubmed-author:IdemaJ GJG
,
pubmed-author:PlasmanJ WJW
,
pubmed-author:SykesMM
pubmed:issnType
Print
pubmed:volume
26 Suppl 1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1-2
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:7737253-Delayed-Action Preparations
,
pubmed-meshheading:7737253-Drug Administration Schedule
,
pubmed-meshheading:7737253-Goserelin
,
pubmed-meshheading:7737253-Humans
,
pubmed-meshheading:7737253-Injections, Subcutaneous
,
pubmed-meshheading:7737253-Male
,
pubmed-meshheading:7737253-Prostatic Neoplasms
pubmed:year
1994
pubmed:articleTitle
A phase III randomized trial comparing the efficacy and safety of the 3-monthly 10.8-mg depot of Zoladex with the monthly 3.6-mg depot in patients with advanced prostate cancer. Dutch South East Cooperative Urological Group.
pubmed:affiliation
Department of Urology, St. Ignatius Hospital, Breda, The Netherlands.
pubmed:publicationType
Journal Article
,
Clinical Trial
,
Comparative Study
,
Randomized Controlled Trial
,
Research Support, Non-U.S. Gov't
,
Clinical Trial, Phase III