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19372299
Source:
http://linkedlifedata.com/resource/pubmed/id/19372299
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55
)
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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:C0030761
,
umls-concept:C0205210
,
umls-concept:C0332257
,
umls-concept:C0338451
,
umls-concept:C1368019
,
umls-concept:C1421437
,
umls-concept:C1833662
,
umls-concept:C1833672
,
umls-concept:C1843663
,
umls-concept:C2348519
pubmed:issue
5
pubmed:dateCreated
2009-4-17
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/2985191R
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA
,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides
,
http://linkedlifedata.com/resource/pubmed/chemical/valosin
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1468-330X
pubmed:author
pubmed-author:BarresiRR
,
pubmed-author:CleggSS
,
pubmed-author:EugenicosMM
,
pubmed-author:JacksonA PAP
,
pubmed-author:MillerT DTD
,
pubmed-author:SmartC MCM
,
pubmed-author:StoneJJ
,
pubmed-author:StraubVV
,
pubmed-author:SummersDD
pubmed:issnType
Electronic
pubmed:volume
80
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
583-4
pubmed:meshHeading
pubmed-meshheading:19372299-Adult
,
pubmed-meshheading:19372299-DNA
,
pubmed-meshheading:19372299-DNA Mutational Analysis
,
pubmed-meshheading:19372299-Dementia
,
pubmed-meshheading:19372299-Female
,
pubmed-meshheading:19372299-Humans
,
pubmed-meshheading:19372299-Magnetic Resonance Imaging
,
pubmed-meshheading:19372299-Male
,
pubmed-meshheading:19372299-Middle Aged
,
pubmed-meshheading:19372299-Muscle Weakness
,
pubmed-meshheading:19372299-Myositis, Inclusion Body
,
pubmed-meshheading:19372299-Osteitis Deformans
,
pubmed-meshheading:19372299-Pedigree
,
pubmed-meshheading:19372299-Peptides
,
pubmed-meshheading:19372299-Urinary Incontinence, Urge
,
pubmed-meshheading:19372299-Young Adult
pubmed:year
2009
pubmed:articleTitle
Inclusion body myopathy with Paget disease and frontotemporal dementia (IBMPFD): clinical features including sphincter disturbance in a large pedigree.
pubmed:publicationType
Letter