19380697

Source:http://linkedlifedata.com/resource/pubmed/id/19380697

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0087012, umls-concept:C0242422, umls-concept:C0332307, umls-concept:C0919453
pubmed:issue	16
pubmed:dateCreated	2009-4-21
pubmed:abstractText	To investigate the role of spinocerebellar ataxia type 17 (SCA17) in the development of parkinsonism.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers, http://linkedlifedata.com/resource/pubmed/chemical/Dopamine Plasma Membrane Transport..., http://linkedlifedata.com/resource/pubmed/chemical/Organotechnetium Compounds, http://linkedlifedata.com/resource/pubmed/chemical/TATA-Box Binding Protein, http://linkedlifedata.com/resource/pubmed/chemical/TBP protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Tropanes, http://linkedlifedata.com/resource/pubmed/chemical/technetium Tc 99m TRODAT-1
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1526-632X
pubmed:author	pubmed-author:JeonB SBS, pubmed-author:KimJ SJS, pubmed-author:KimJ YJY, pubmed-author:KimJ-MJM, pubmed-author:KimJ-YJY, pubmed-author:KimS ESE, pubmed-author:KimS YSY, pubmed-author:KimY KYK, pubmed-author:LeiB WBW, pubmed-author:NacuII, pubmed-author:ParkS SSS, pubmed-author:ZengX NXN
pubmed:issnType	Electronic
pubmed:day	21
pubmed:volume	72
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1385-9
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:19380697-Aged, pubmed-meshheading:19380697-Biological Markers, pubmed-meshheading:19380697-Corpus Striatum, pubmed-meshheading:19380697-DNA Mutational Analysis, pubmed-meshheading:19380697-Dopamine Plasma Membrane Transport Proteins, pubmed-meshheading:19380697-Female, pubmed-meshheading:19380697-Gene Frequency, pubmed-meshheading:19380697-Genetic Predisposition to Disease, pubmed-meshheading:19380697-Genetic Testing, pubmed-meshheading:19380697-Genotype, pubmed-meshheading:19380697-Humans, pubmed-meshheading:19380697-Male, pubmed-meshheading:19380697-Middle Aged, pubmed-meshheading:19380697-Multiple System Atrophy, pubmed-meshheading:19380697-Mutation, pubmed-meshheading:19380697-Organotechnetium Compounds, pubmed-meshheading:19380697-Parkinsonian Disorders, pubmed-meshheading:19380697-Predictive Value of Tests, pubmed-meshheading:19380697-Substantia Nigra, pubmed-meshheading:19380697-TATA-Box Binding Protein, pubmed-meshheading:19380697-Tomography, Emission-Computed, Single-Photon, pubmed-meshheading:19380697-Tropanes
pubmed:year	2009
pubmed:articleTitle	Spinocerebellar ataxia type 17 mutation as a causative and susceptibility gene in parkinsonism.
pubmed:affiliation	Department of Neurology, Neuroscience Research Institute, Korea.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't