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18372408
Source:
http://linkedlifedata.com/resource/pubmed/id/18372408
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0009221
,
umls-concept:C0012222
,
umls-concept:C0017431
,
umls-concept:C0022336
,
umls-concept:C0030705
,
umls-concept:C0042295
,
umls-concept:C1705241
,
umls-concept:C1705242
,
umls-concept:C1707429
pubmed:issue
7
pubmed:dateCreated
2008-8-14
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18372408-12748093
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/8003708
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Codon
,
http://linkedlifedata.com/resource/pubmed/chemical/Methionine
,
http://linkedlifedata.com/resource/pubmed/chemical/Prions
,
http://linkedlifedata.com/resource/pubmed/chemical/Valine
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1936-959X
pubmed:author
pubmed-author:BrandelJ PJP
,
pubmed-author:ChirasJJ
,
pubmed-author:DormontDD
,
pubmed-author:GalanaudDD
,
pubmed-author:HeryBB
,
pubmed-author:RanjevaJ PJP
pubmed:issnType
Electronic
pubmed:volume
29
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
E57; author reply E58
pubmed:meshHeading
pubmed-meshheading:18372408-Basal Ganglia
,
pubmed-meshheading:18372408-Caudate Nucleus
,
pubmed-meshheading:18372408-Cerebral Cortex
,
pubmed-meshheading:18372408-Codon
,
pubmed-meshheading:18372408-Corpus Striatum
,
pubmed-meshheading:18372408-Creutzfeldt-Jakob Syndrome
,
pubmed-meshheading:18372408-Diffusion Magnetic Resonance Imaging
,
pubmed-meshheading:18372408-Genotype
,
pubmed-meshheading:18372408-Humans
,
pubmed-meshheading:18372408-Methionine
,
pubmed-meshheading:18372408-Polymorphism, Genetic
,
pubmed-meshheading:18372408-Prions
,
pubmed-meshheading:18372408-Pulvinar
,
pubmed-meshheading:18372408-Retrospective Studies
,
pubmed-meshheading:18372408-Valine
pubmed:year
2008
pubmed:articleTitle
Differences of apparent diffusion coefficient values in patients with Creutzfeldt-Jakob disease according to the codon 129 genotype.
pubmed:publicationType
Letter
,
Comment