SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
16437559
Source:
http://linkedlifedata.com/resource/pubmed/id/16437559
Search
Subject
(
57
)
Predicate
Object
All
Download in:
JSON
RDF
N3/Turtle
N-Triples
Switch to
Custom View
Named Graph
All
UniProt
NCBIGene
DrugBank
ClinicalTrials
UMLS
PubMed
Mappings
MentionedEntities
Language
All
English
Español
Português
Français
Deutsch
Русский
日本語
Български
Inference
Explicit and implicit
Explicit only
Implicit only
Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0752347
,
umls-concept:C1425650
pubmed:issue
2
pubmed:dateCreated
2006-1-31
pubmed:abstractText
The Lrrk2 kinase domain G2019S substitution is the most common genetic basis of familial and sporadic parkinsonism. Patients harboring the G2019S substitution usually present with clinical Parkinson's disease.
pubmed:grant
http://linkedlifedata.com/resource/pubmed/grant/P01 AG17216
,
http://linkedlifedata.com/resource/pubmed/grant/P50 NS40256
,
http://linkedlifedata.com/resource/pubmed/grant/R01 ES013941
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/7707449
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Glycine
,
http://linkedlifedata.com/resource/pubmed/chemical/LRRK2 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases
,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/serin-rich spermatogenic protein...
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0364-5134
pubmed:author
pubmed-author:DicksonDennis WDW
,
pubmed-author:FarrerMatthew JMJ
,
pubmed-author:GordonMark FMF
,
pubmed-author:JohnsonJoseph LJL
,
pubmed-author:LitvanIreneI
,
pubmed-author:MashDeborah CDC
,
pubmed-author:PapapetropoulosSpiridonS
,
pubmed-author:RossOwen AOA
,
pubmed-author:ToftMathiasM
,
pubmed-author:WhittleAndrew JAJ
,
pubmed-author:WszolekZbigniew KZK
pubmed:issnType
Print
pubmed:volume
59
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
388-93
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:16437559-Aged
,
pubmed-meshheading:16437559-Aged, 80 and over
,
pubmed-meshheading:16437559-Brain Stem
,
pubmed-meshheading:16437559-DNA Mutational Analysis
,
pubmed-meshheading:16437559-Female
,
pubmed-meshheading:16437559-Glycine
,
pubmed-meshheading:16437559-Humans
,
pubmed-meshheading:16437559-Lewy Body Disease
,
pubmed-meshheading:16437559-Male
,
pubmed-meshheading:16437559-Models, Molecular
,
pubmed-meshheading:16437559-Mutation
,
pubmed-meshheading:16437559-Protein-Serine-Threonine Kinases
,
pubmed-meshheading:16437559-Proteins
pubmed:year
2006
pubmed:articleTitle
Lrrk2 and Lewy body disease.
pubmed:affiliation
Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, FL 32224, USA.
pubmed:publicationType
Journal Article
,
Comparative Study
,
Research Support, Non-U.S. Gov't
,
Research Support, N.I.H., Extramural