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15079038
Source:
http://linkedlifedata.com/resource/pubmed/id/15079038
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59
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0004083
,
umls-concept:C0030567
,
umls-concept:C0231449
,
umls-concept:C0796357
,
umls-concept:C1417836
,
umls-concept:C2603343
pubmed:issue
7
pubmed:dateCreated
2004-4-13
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/NR4A2 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Receptor Subfamily 4...
,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1526-632X
pubmed:author
pubmed-author:BauerPP
,
pubmed-author:BergDD
,
pubmed-author:BergerKK
,
pubmed-author:HeringRR
,
pubmed-author:HolzmannCC
,
pubmed-author:KrügerRR
,
pubmed-author:MüllerTT
,
pubmed-author:MilesP DPD
,
pubmed-author:PetrovicSS
,
pubmed-author:RieszTT
,
pubmed-author:WoitallaDD
pubmed:issnType
Electronic
pubmed:day
13
pubmed:volume
62
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1231-2
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:15079038-Aged
,
pubmed-meshheading:15079038-Cohort Studies
,
pubmed-meshheading:15079038-DNA Mutational Analysis
,
pubmed-meshheading:15079038-DNA-Binding Proteins
,
pubmed-meshheading:15079038-Exons
,
pubmed-meshheading:15079038-Female
,
pubmed-meshheading:15079038-Gene Frequency
,
pubmed-meshheading:15079038-Genotype
,
pubmed-meshheading:15079038-Humans
,
pubmed-meshheading:15079038-Introns
,
pubmed-meshheading:15079038-Male
,
pubmed-meshheading:15079038-Middle Aged
,
pubmed-meshheading:15079038-Nuclear Receptor Subfamily 4, Group A, Member 2
,
pubmed-meshheading:15079038-Parkinson Disease
,
pubmed-meshheading:15079038-Polymorphism, Genetic
,
pubmed-meshheading:15079038-Psychotic Disorders
,
pubmed-meshheading:15079038-Transcription Factors
pubmed:year
2004
pubmed:articleTitle
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease.
pubmed:affiliation
Department of Medical Genetics, Hertie Institute of Clinical Brain Research, University of Tübingen, Germany.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't