19012866

Source:http://linkedlifedata.com/resource/pubmed/id/19012866

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015127, umls-concept:C0015576, umls-concept:C0026882, umls-concept:C0338451, umls-concept:C1314792, umls-concept:C1415311, umls-concept:C1710263
pubmed:issue	6
pubmed:dateCreated	2008-11-17
pubmed:abstractText	Frontotemporal dementia (FTD) is a neurodegenerative disease characterized by cognitive impairment, language dysfunction, and/or changes in personality. Recently it has been shown that progranulin (GRN) mutations can cause FTD as well as other neurodegenerative phenotypes.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101231978
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/GRN protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Signaling Peptides...
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	1552-5279
pubmed:author	pubmed-author:AxelmanKarinK, pubmed-author:BjörkBehnosh FBF, pubmed-author:BrohedeJesperJ, pubmed-author:ChiangHuei-HsinHH, pubmed-author:GraffCarolineC, pubmed-author:NennesmoIngerI, pubmed-author:RobinsTiinaT, pubmed-author:RosvallLinaL
pubmed:issnType	Electronic
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	414-20
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:19012866-Age of Onset, pubmed-meshheading:19012866-Aged, pubmed-meshheading:19012866-Cognition Disorders, pubmed-meshheading:19012866-DNA Mutational Analysis, pubmed-meshheading:19012866-Dementia, pubmed-meshheading:19012866-European Continental Ancestry Group, pubmed-meshheading:19012866-Frameshift Mutation, pubmed-meshheading:19012866-Frontal Lobe, pubmed-meshheading:19012866-Genetic Predisposition to Disease, pubmed-meshheading:19012866-Genetic Testing, pubmed-meshheading:19012866-Humans, pubmed-meshheading:19012866-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:19012866-Magnetic Resonance Imaging, pubmed-meshheading:19012866-Middle Aged, pubmed-meshheading:19012866-Neurodegenerative Diseases, pubmed-meshheading:19012866-Neuropsychological Tests, pubmed-meshheading:19012866-Pedigree, pubmed-meshheading:19012866-Phenotype, pubmed-meshheading:19012866-Sweden, pubmed-meshheading:19012866-Temporal Lobe
pubmed:year	2008
pubmed:articleTitle	Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family.
pubmed:affiliation	Karolinska Institutet, Department NVS, KI-Alzheimer Disease Research Center, Novum, Huddinge, Stockholm, Sweden.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't