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18229654
Source:
http://linkedlifedata.com/resource/pubmed/id/18229654
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pubmed-article:18229654
rdf:type
pubmed:Citation
lld:pubmed
pubmed-article:18229654
lifeskim:mentions
umls-concept:C0026848
lld:lifeskim
pubmed-article:18229654
lifeskim:mentions
umls-concept:C1457887
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pubmed-article:18229654
lifeskim:mentions
umls-concept:C0015576
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pubmed-article:18229654
lifeskim:mentions
umls-concept:C0220896
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pubmed-article:18229654
lifeskim:mentions
umls-concept:C0684224
lld:lifeskim
pubmed-article:18229654
lifeskim:mentions
umls-concept:C0026882
lld:lifeskim
pubmed-article:18229654
lifeskim:mentions
umls-concept:C1413064
lld:lifeskim
pubmed-article:18229654
lifeskim:mentions
umls-concept:C0332182
lld:lifeskim
pubmed-article:18229654
pubmed:dateCreated
2008-1-30
lld:pubmed
pubmed-article:18229654
pubmed:abstractText
Presenting the case of unusual onset hypokalemic periodic paralysis (HypoPP) where myopathy had developed two years before paralysis occurred.
lld:pubmed
pubmed-article:18229654
pubmed:language
eng
lld:pubmed
pubmed-article:18229654
pubmed:journal
http://linkedlifedata.com/r...
lld:pubmed
pubmed-article:18229654
pubmed:citationSubset
IM
lld:pubmed
pubmed-article:18229654
pubmed:chemical
http://linkedlifedata.com/r...
lld:pubmed
pubmed-article:18229654
pubmed:chemical
http://linkedlifedata.com/r...
lld:pubmed
pubmed-article:18229654
pubmed:status
MEDLINE
lld:pubmed
pubmed-article:18229654
pubmed:issn
1896-1126
lld:pubmed
pubmed-article:18229654
pubmed:author
pubmed-author:BiczyskoWW
lld:pubmed
pubmed-article:18229654
pubmed:author
pubmed-author:WiktorMM
lld:pubmed
pubmed-article:18229654
pubmed:author
pubmed-author:Jurkat-RottKK
lld:pubmed
pubmed-article:18229654
pubmed:author
pubmed-author:SteinbornBB
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pubmed-article:18229654
pubmed:author
pubmed-author:GurdaBB
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pubmed-article:18229654
pubmed:author
pubmed-author:Winczewska-Wi...
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pubmed-article:18229654
pubmed:author
pubmed-author:Lehman-HornFF
lld:pubmed
pubmed-article:18229654
pubmed:issnType
Print
lld:pubmed
pubmed-article:18229654
pubmed:volume
52 Suppl 1
lld:pubmed
pubmed-article:18229654
pubmed:owner
NLM
lld:pubmed
pubmed-article:18229654
pubmed:authorsComplete
Y
lld:pubmed
pubmed-article:18229654
pubmed:pagination
155-7
lld:pubmed
pubmed-article:18229654
pubmed:dateRevised
2008-5-15
lld:pubmed
pubmed-article:18229654
pubmed:meshHeading
pubmed-meshheading:18229654...
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pubmed-article:18229654
pubmed:meshHeading
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pubmed-article:18229654
pubmed:meshHeading
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lld:pubmed
pubmed-article:18229654
pubmed:meshHeading
pubmed-meshheading:18229654...
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pubmed-article:18229654
pubmed:meshHeading
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pubmed-article:18229654
pubmed:meshHeading
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lld:pubmed
pubmed-article:18229654
pubmed:meshHeading
pubmed-meshheading:18229654...
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pubmed-article:18229654
pubmed:meshHeading
pubmed-meshheading:18229654...
lld:pubmed
pubmed-article:18229654
pubmed:meshHeading
pubmed-meshheading:18229654...
lld:pubmed
pubmed-article:18229654
pubmed:meshHeading
pubmed-meshheading:18229654...
lld:pubmed
pubmed-article:18229654
pubmed:year
2007
lld:pubmed
pubmed-article:18229654
pubmed:articleTitle
Myopathy as the first symptom of hypokalemic periodic paralysis--case report of a girl from a Polish family with CACNA1S (R1239G) mutation.
lld:pubmed
pubmed-article:18229654
pubmed:affiliation
Chair and Department of Developmental Neurology, Pozna? University of Medical Sciences, Poland. awwiktor@amp.edu.pl
lld:pubmed
pubmed-article:18229654
pubmed:publicationType
Journal Article
lld:pubmed
pubmed-article:18229654
pubmed:publicationType
Case Reports
lld:pubmed
entrez-gene:779
entrezgene:pubmed
pubmed-article:18229654
lld:entrezgene
http://linkedlifedata.com/r...
entrezgene:pubmed
pubmed-article:18229654
lld:entrezgene
lhgdn:association:10408
lhgdn:found_in
pubmed-article:18229654
lld:lhgdn