SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
18195218
Source:
http://linkedlifedata.com/resource/pubmed/id/18195218
Search
Subject
(
59
)
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:C0013867
,
umls-concept:C0031437
,
umls-concept:C0039082
,
umls-concept:C0205210
,
umls-concept:C1706089
,
umls-concept:C2827666
pubmed:issue
1
pubmed:dateCreated
2008-1-15
pubmed:abstractText
To characterize the clinical phenotype and to study the course of disease in patients with Alström syndrome, with an emphasis on retinal function assessed with full-field electroretinography (ERG).
pubmed:grant
http://linkedlifedata.com/resource/pubmed/grant/EY08683
,
http://linkedlifedata.com/resource/pubmed/grant/HD036878
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/7706534
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/ALMS1 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0003-9950
pubmed:author
pubmed-author:AndréassonStenS
,
pubmed-author:HinmanElizabeth GEG
,
pubmed-author:MöllerClaesC
,
pubmed-author:MalmEvaE
,
pubmed-author:MarshallJan DJD
,
pubmed-author:NaggertJürgen KJK
,
pubmed-author:NishinaPatsy MPM
,
pubmed-author:PonjavicVesnaV
pubmed:issnType
Print
pubmed:volume
126
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
51-7
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:18195218-Abnormalities, Multiple
,
pubmed-meshheading:18195218-Child
,
pubmed-meshheading:18195218-Color Vision Defects
,
pubmed-meshheading:18195218-DNA Mutational Analysis
,
pubmed-meshheading:18195218-Electroretinography
,
pubmed-meshheading:18195218-Female
,
pubmed-meshheading:18195218-Hearing Loss, Sensorineural
,
pubmed-meshheading:18195218-Humans
,
pubmed-meshheading:18195218-Mutation
,
pubmed-meshheading:18195218-Obesity
,
pubmed-meshheading:18195218-Phenotype
,
pubmed-meshheading:18195218-Photoreceptor Cells, Vertebrate
,
pubmed-meshheading:18195218-Polymerase Chain Reaction
,
pubmed-meshheading:18195218-Proteins
,
pubmed-meshheading:18195218-Retinitis Pigmentosa
,
pubmed-meshheading:18195218-Syndrome
,
pubmed-meshheading:18195218-Vision Disorders
,
pubmed-meshheading:18195218-Visual Field Tests
,
pubmed-meshheading:18195218-Visual Fields
pubmed:year
2008
pubmed:articleTitle
Full-field electroretinography and marked variability in clinical phenotype of Alström syndrome.
pubmed:affiliation
Department of Ophthalmology, Lund University Hospital, SE-221 85, Lund, Sweden. eva.malm@med.lu.se
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't
,
Research Support, N.I.H., Extramural