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15073448
Source:
http://linkedlifedata.com/resource/pubmed/id/15073448
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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:C0026882
,
umls-concept:C0030705
,
umls-concept:C0031437
,
umls-concept:C0205280
,
umls-concept:C1537041
,
umls-concept:C1850620
pubmed:issue
3
pubmed:dateCreated
2004-5-10
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0150760
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
,
http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin-Protein Ligases
,
http://linkedlifedata.com/resource/pubmed/chemical/parkin protein
pubmed:status
MEDLINE
pubmed:issn
0014-3022
pubmed:author
pubmed-author:KosakaMasaakiM
,
pubmed-author:KunishigeMakotoM
,
pubmed-author:KurodaYukikoY
,
pubmed-author:MatsumotoToshioT
,
pubmed-author:MitsuiTakaoT
,
pubmed-author:YoshidaSumikoS
pubmed:issnType
Print
pubmed:volume
51
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
183-5
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15073448-Blotting, Southern
,
pubmed-meshheading:15073448-Brain
,
pubmed-meshheading:15073448-Cerebellar Ataxia
,
pubmed-meshheading:15073448-DNA Mutational Analysis
,
pubmed-meshheading:15073448-Exons
,
pubmed-meshheading:15073448-Family Health
,
pubmed-meshheading:15073448-Female
,
pubmed-meshheading:15073448-Heterozygote
,
pubmed-meshheading:15073448-Humans
,
pubmed-meshheading:15073448-Magnetic Resonance Imaging
,
pubmed-meshheading:15073448-Male
,
pubmed-meshheading:15073448-Middle Aged
,
pubmed-meshheading:15073448-Mutation
,
pubmed-meshheading:15073448-Parkinsonian Disorders
,
pubmed-meshheading:15073448-Phenotype
,
pubmed-meshheading:15073448-RNA, Messenger
,
pubmed-meshheading:15073448-Reverse Transcriptase Polymerase Chain Reaction
,
pubmed-meshheading:15073448-Ubiquitin-Protein Ligases
pubmed:year
2004
pubmed:articleTitle
Expanding phenotype and clinical heterogeneity in patients with identical mutation of the parkin gene.
pubmed:affiliation
Department of Medicine and Bioregulatory Sciences, University of Tokushima Graduate School of Medicine, Tokushima, Japan. kuni@clin.med.tokushima-u.ac.jp
pubmed:publicationType
Journal Article
,
Comparative Study