18211709

Source:http://linkedlifedata.com/resource/pubmed/id/18211709

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0030567, umls-concept:C0030705, umls-concept:C0032729, umls-concept:C0936012, umls-concept:C1418270, umls-concept:C1420276, umls-concept:C1422771, umls-concept:C1425650
pubmed:dateCreated	2008-2-20
pubmed:abstractText	Mutations in the genes PRKN and LRRK2 are the most frequent known genetic lesions among Parkinson's disease patients. We have previously reported that in the Portuguese population the LRRK2 c.6055G > A; p.G2019S mutation has one of the highest frequencies in Europe.
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-11835383, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-12210852, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-12446870, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-12953260, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-12971891, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-14593171, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-14872018, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-15087508, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-15349870, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-15365989, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-15541308, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-15541309, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-1564476, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-15895422, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-16149095, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-16311269, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-16436781, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-16436782, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-17027339, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-17095157, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-9197268, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-9560156, http://linkedlifedata.com/resource/pubmed/commentcorrection/18211709-9923759
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100968555
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/LRRK2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Methionine, http://linkedlifedata.com/resource/pubmed/chemical/PTEN-induced putative kinase, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/SNCA protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Threonine, http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin-Protein Ligases, http://linkedlifedata.com/resource/pubmed/chemical/alpha-Synuclein, http://linkedlifedata.com/resource/pubmed/chemical/parkin protein
pubmed:status	MEDLINE
pubmed:issn	1471-2377
pubmed:author	pubmed-author:BrasJoseJ, pubmed-author:CaladoAnaA, pubmed-author:DiasMargaridaM, pubmed-author:GuerreiroRitaR, pubmed-author:HardyJohnJ, pubmed-author:JanuarioCristinaC, pubmed-author:MorgadinhoAnaA, pubmed-author:OliveiraCatarinaC, pubmed-author:RibeiroMariaM, pubmed-author:SemedoCristinaC, pubmed-author:SingletonAndrewA
pubmed:issnType	Electronic
pubmed:volume	8
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:18211709-Aged, pubmed-meshheading:18211709-DNA Mutational Analysis, pubmed-meshheading:18211709-Exons, pubmed-meshheading:18211709-Family Health, pubmed-meshheading:18211709-Female, pubmed-meshheading:18211709-Genetic Predisposition to Disease, pubmed-meshheading:18211709-Humans, pubmed-meshheading:18211709-Male, pubmed-meshheading:18211709-Methionine, pubmed-meshheading:18211709-Middle Aged, pubmed-meshheading:18211709-Mutation, pubmed-meshheading:18211709-Parkinson Disease, pubmed-meshheading:18211709-Portugal, pubmed-meshheading:18211709-Protein Kinases, pubmed-meshheading:18211709-Protein-Serine-Threonine Kinases, pubmed-meshheading:18211709-Threonine, pubmed-meshheading:18211709-Ubiquitin-Protein Ligases, pubmed-meshheading:18211709-alpha-Synuclein
pubmed:year	2008
pubmed:articleTitle	Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2.
pubmed:affiliation	Center for Neurosciences and Cell Biology, Faculty of Medicine, University of Coimbra, Coimbra, Portugal. brasj@nia.nih.gov
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Intramural