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19808383
Source:
http://linkedlifedata.com/resource/pubmed/id/19808383
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58
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0018787
,
umls-concept:C0018801
,
umls-concept:C0026882
,
umls-concept:C0152025
,
umls-concept:C0205210
,
umls-concept:C0205409
,
umls-concept:C0220912
,
umls-concept:C0220913
,
umls-concept:C0678226
,
umls-concept:C1280464
,
umls-concept:C1314939
,
umls-concept:C1832428
,
umls-concept:C2751492
pubmed:issue
5
pubmed:dateCreated
2009-10-7
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/101479941
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Methionine
,
http://linkedlifedata.com/resource/pubmed/chemical/Prealbumin
,
http://linkedlifedata.com/resource/pubmed/chemical/Valine
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1941-3297
pubmed:author
pubmed-author:BabaHideo AHA
,
pubmed-author:BoeseDirkD
,
pubmed-author:ChristophDaniel CDC
,
pubmed-author:ErbelRaimundR
,
pubmed-author:HunoldPeterP
,
pubmed-author:JohnsonKristian T MKT
,
pubmed-author:PhilippSebastianS
,
pubmed-author:SchlosserThomas WTW
pubmed:issnType
Electronic
pubmed:volume
2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
512-5
pubmed:meshHeading
pubmed-meshheading:19808383-Amyloidosis, Familial
,
pubmed-meshheading:19808383-Cardiomyopathies
,
pubmed-meshheading:19808383-Echocardiography
,
pubmed-meshheading:19808383-Heart Failure
,
pubmed-meshheading:19808383-Humans
,
pubmed-meshheading:19808383-Immunohistochemistry
,
pubmed-meshheading:19808383-Magnetic Resonance Imaging
,
pubmed-meshheading:19808383-Male
,
pubmed-meshheading:19808383-Methionine
,
pubmed-meshheading:19808383-Microscopy, Electron
,
pubmed-meshheading:19808383-Middle Aged
,
pubmed-meshheading:19808383-Mutation
,
pubmed-meshheading:19808383-Prealbumin
,
pubmed-meshheading:19808383-Valine
pubmed:year
2009
pubmed:articleTitle
Heart failure and cardiac involvement as isolated manifestation of familial form of transthyretin amyloidosis resulting from Val30Met mutation with no clinical signs of polyneuropathy.
pubmed:affiliation
Department of Oncology, West German Cancer Center, University Hospital of Essen, Germany.
pubmed:publicationType
Journal Article
,
Case Reports
,
Research Support, Non-U.S. Gov't