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21029358
Source:
http://linkedlifedata.com/resource/pubmed/id/21029358
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55
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0017337
,
umls-concept:C0032105
,
umls-concept:C0035647
,
umls-concept:C0042487
,
umls-concept:C0205419
,
umls-concept:C0332281
,
umls-concept:C0441889
,
umls-concept:C1336938
,
umls-concept:C1366370
,
umls-concept:C1704822
,
umls-concept:C2732002
pubmed:issue
1
pubmed:dateCreated
2011-1-7
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/101170508
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers
,
http://linkedlifedata.com/resource/pubmed/chemical/Factor VIII
,
http://linkedlifedata.com/resource/pubmed/chemical/von Willebrand Factor
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1538-7836
pubmed:author
pubmed-author:AntoniGG
,
pubmed-author:EmmerichJJ
,
pubmed-author:MorangeP-EPE
,
pubmed-author:SaulFF
,
pubmed-author:TrégouëtD-ADA
pubmed:issnType
Electronic
pubmed:volume
9
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
229-31
pubmed:meshHeading
pubmed-meshheading:21029358-Biological Markers
,
pubmed-meshheading:21029358-Case-Control Studies
,
pubmed-meshheading:21029358-Factor VIII
,
pubmed-meshheading:21029358-Female
,
pubmed-meshheading:21029358-France
,
pubmed-meshheading:21029358-Gene Frequency
,
pubmed-meshheading:21029358-Genetic Predisposition to Disease
,
pubmed-meshheading:21029358-Genome-Wide Association Study
,
pubmed-meshheading:21029358-Humans
,
pubmed-meshheading:21029358-Logistic Models
,
pubmed-meshheading:21029358-Male
,
pubmed-meshheading:21029358-Odds Ratio
,
pubmed-meshheading:21029358-Phenotype
,
pubmed-meshheading:21029358-Polymorphism, Single Nucleotide
,
pubmed-meshheading:21029358-Risk Assessment
,
pubmed-meshheading:21029358-Risk Factors
,
pubmed-meshheading:21029358-Venous Thrombosis
,
pubmed-meshheading:21029358-von Willebrand Factor
pubmed:year
2011
pubmed:articleTitle
Impact on venous thrombosis risk of newly discovered gene variants associated with FVIII and VWF plasma levels.
pubmed:publicationType
Letter
,
Research Support, Non-U.S. Gov't