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19844732
Source:
http://linkedlifedata.com/resource/pubmed/id/19844732
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51
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0008666
,
umls-concept:C0026882
,
umls-concept:C0030664
,
umls-concept:C0208973
,
umls-concept:C0332197
,
umls-concept:C0338451
,
umls-concept:C1314792
,
umls-concept:C1517892
,
umls-concept:C1538456
,
umls-concept:C1704666
pubmed:issue
5
pubmed:dateCreated
2010-1-20
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0412041
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CHMP2B protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Endosomal Sorting Complexes...
,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Protein FUS
,
http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1432-0533
pubmed:author
pubmed-author:HolmIda ElisabethIE
,
pubmed-author:IsaacsAdrian MAM
,
pubmed-author:MackenzieIan R AIR
pubmed:issnType
Electronic
pubmed:volume
118
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
719-20
pubmed:meshHeading
pubmed-meshheading:19844732-Aged
,
pubmed-meshheading:19844732-Brain
,
pubmed-meshheading:19844732-Chromosomes, Human, Pair 3
,
pubmed-meshheading:19844732-Endosomal Sorting Complexes Required for Transport
,
pubmed-meshheading:19844732-Female
,
pubmed-meshheading:19844732-Frontotemporal Dementia
,
pubmed-meshheading:19844732-Humans
,
pubmed-meshheading:19844732-Inclusion Bodies
,
pubmed-meshheading:19844732-Male
,
pubmed-meshheading:19844732-Middle Aged
,
pubmed-meshheading:19844732-Mutation
,
pubmed-meshheading:19844732-Nerve Tissue Proteins
,
pubmed-meshheading:19844732-Pedigree
,
pubmed-meshheading:19844732-Postmortem Changes
,
pubmed-meshheading:19844732-RNA-Binding Protein FUS
,
pubmed-meshheading:19844732-Ubiquitin
pubmed:year
2009
pubmed:articleTitle
Absence of FUS-immunoreactive pathology in frontotemporal dementia linked to chromosome 3 (FTD-3) caused by mutation in the CHMP2B gene.
pubmed:publicationType
Letter