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16362832
Source:
http://linkedlifedata.com/resource/pubmed/id/16362832
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56
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Inference
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0011164
,
umls-concept:C0017337
,
umls-concept:C0026882
,
umls-concept:C0031437
,
umls-concept:C0241888
,
umls-concept:C0443147
,
umls-concept:C1707959
,
umls-concept:C1720655
,
umls-concept:C1947974
,
umls-concept:C2700455
,
umls-concept:C2827666
pubmed:issue
12
pubmed:dateCreated
2005-12-19
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0423161
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Proline
,
http://linkedlifedata.com/resource/pubmed/chemical/Serine
,
http://linkedlifedata.com/resource/pubmed/chemical/tau Proteins
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0340-5354
pubmed:author
pubmed-author:AzulayJ PJP
,
pubmed-author:CasseronWW
,
pubmed-author:GastautJ LJL
,
pubmed-author:GuedjEE
,
pubmed-author:PougetJJ
pubmed:issnType
Print
pubmed:volume
252
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1546-8
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:16362832-Adult
,
pubmed-meshheading:16362832-Basal Ganglia
,
pubmed-meshheading:16362832-Cerebral Cortex
,
pubmed-meshheading:16362832-DNA Mutational Analysis
,
pubmed-meshheading:16362832-Family Health
,
pubmed-meshheading:16362832-Humans
,
pubmed-meshheading:16362832-Machado-Joseph Disease
,
pubmed-meshheading:16362832-Magnetic Resonance Imaging
,
pubmed-meshheading:16362832-Male
,
pubmed-meshheading:16362832-Middle Aged
,
pubmed-meshheading:16362832-Mutation
,
pubmed-meshheading:16362832-Pedigree
,
pubmed-meshheading:16362832-Phenotype
,
pubmed-meshheading:16362832-Proline
,
pubmed-meshheading:16362832-Serine
,
pubmed-meshheading:16362832-Tomography, Emission-Computed, Single-Photon
,
pubmed-meshheading:16362832-tau Proteins
pubmed:year
2005
pubmed:articleTitle
Familial autosomal dominant cortico-basal degeneration with the P301S mutation in the tau gene: an example of phenotype variability.
pubmed:publicationType
Letter
,
Comparative Study
,
Case Reports