SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
19187823
Source:
http://linkedlifedata.com/resource/pubmed/id/19187823
Search
Subject
(
48
)
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:C0009219
,
umls-concept:C0017337
,
umls-concept:C0056207
,
umls-concept:C0205419
,
umls-concept:C0332281
pubmed:issue
2
pubmed:dateCreated
2009-2-3
pubmed:abstractText
To investigate whether variants in the complement factor H (CFH) gene are associated with polypoidal choroidal vasculopathy (PCV).
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/7802443
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Complement Factor H
,
http://linkedlifedata.com/resource/pubmed/chemical/complement factor H, human
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1549-4713
pubmed:author
pubmed-author:HondaShigeruS
,
pubmed-author:KondoNaoshiN
,
pubmed-author:KunoShin-ichiS
,
pubmed-author:NegiAkiraA
pubmed:issnType
Electronic
pubmed:volume
116
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
304-10
pubmed:meshHeading
pubmed-meshheading:19187823-Aged
,
pubmed-meshheading:19187823-Aged, 80 and over
,
pubmed-meshheading:19187823-Case-Control Studies
,
pubmed-meshheading:19187823-Choroid
,
pubmed-meshheading:19187823-Choroid Diseases
,
pubmed-meshheading:19187823-Complement Factor H
,
pubmed-meshheading:19187823-Cross-Sectional Studies
,
pubmed-meshheading:19187823-Female
,
pubmed-meshheading:19187823-Genotype
,
pubmed-meshheading:19187823-Haplotypes
,
pubmed-meshheading:19187823-Humans
,
pubmed-meshheading:19187823-Linkage Disequilibrium
,
pubmed-meshheading:19187823-Male
,
pubmed-meshheading:19187823-Middle Aged
,
pubmed-meshheading:19187823-Open Reading Frames
,
pubmed-meshheading:19187823-Peripheral Vascular Diseases
,
pubmed-meshheading:19187823-Polymorphism, Single Nucleotide
pubmed:year
2009
pubmed:articleTitle
Coding variant I62V in the complement factor H gene is strongly associated with polypoidal choroidal vasculopathy.
pubmed:affiliation
Department of Surgery, Division of Ophthalmology, Kobe University Graduate School of Medicine, Kobe, Japan.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't