SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
14757870
Source:
http://linkedlifedata.com/resource/pubmed/id/14757870
Search
Subject
(
56
)
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:C0026882
,
umls-concept:C0152200
,
umls-concept:C0205314
,
umls-concept:C0679622
,
umls-concept:C1314792
,
umls-concept:C1413545
,
umls-concept:C1413548
pubmed:issue
2
pubmed:dateCreated
2004-2-3
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CNGB3 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic Nucleotide-Gated Cation...
,
http://linkedlifedata.com/resource/pubmed/chemical/Ion Channels
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1468-6244
pubmed:author
pubmed-author:AinsworthJ RJR
,
pubmed-author:AligianisI AIA
,
pubmed-author:HuntD MDM
,
pubmed-author:JohnsonSS
,
pubmed-author:MaherE RER
,
pubmed-author:MichaelidesMM
,
pubmed-author:MollonJ DJD
,
pubmed-author:MooreA TAT
pubmed:issnType
Electronic
pubmed:volume
41
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
e20
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:14757870-Adolescent
,
pubmed-meshheading:14757870-Adult
,
pubmed-meshheading:14757870-Aged
,
pubmed-meshheading:14757870-Amino Acid Substitution
,
pubmed-meshheading:14757870-Child
,
pubmed-meshheading:14757870-Child, Preschool
,
pubmed-meshheading:14757870-Color Vision Defects
,
pubmed-meshheading:14757870-Cyclic Nucleotide-Gated Cation Channels
,
pubmed-meshheading:14757870-DNA Mutational Analysis
,
pubmed-meshheading:14757870-Female
,
pubmed-meshheading:14757870-Genotype
,
pubmed-meshheading:14757870-Humans
,
pubmed-meshheading:14757870-Ion Channels
,
pubmed-meshheading:14757870-Male
,
pubmed-meshheading:14757870-Middle Aged
,
pubmed-meshheading:14757870-Mutation
,
pubmed-meshheading:14757870-Polymorphism, Single Nucleotide
pubmed:year
2004
pubmed:articleTitle
Achromatopsia caused by novel mutations in both CNGA3 and CNGB3.
pubmed:affiliation
Institute of Ophthalmology, University College London, 11-43 Bath Street, London EC1V 9EV, UK.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't
,
Multicenter Study