SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
11217940
Source:
http://linkedlifedata.com/resource/pubmed/id/11217940
Search
Subject
(
51
)
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:C0013865
,
umls-concept:C0017337
,
umls-concept:C0026882
,
umls-concept:C0205314
,
umls-concept:C0271091
,
umls-concept:C0332281
,
umls-concept:C0679622
,
umls-concept:C0920367
,
umls-concept:C1419764
pubmed:issue
1
pubmed:dateCreated
2001-2-19
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/8309919
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Eye Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/RS1 protein, human
pubmed:status
MEDLINE
pubmed:issn
0275-004X
pubmed:author
pubmed-author:ChongN HNH
,
pubmed-author:HardcastleA JAJ
,
pubmed-author:HolderG EGE
,
pubmed-author:ReedB KBK
,
pubmed-author:StangaP EPE
pubmed:issnType
Print
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
78-80
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:11217940-Adult
,
pubmed-meshheading:11217940-DNA Mutational Analysis
,
pubmed-meshheading:11217940-Electroretinography
,
pubmed-meshheading:11217940-Eye Diseases, Hereditary
,
pubmed-meshheading:11217940-Eye Proteins
,
pubmed-meshheading:11217940-Genetic Linkage
,
pubmed-meshheading:11217940-Humans
,
pubmed-meshheading:11217940-Male
,
pubmed-meshheading:11217940-Mutation
,
pubmed-meshheading:11217940-Polymerase Chain Reaction
,
pubmed-meshheading:11217940-Retina
,
pubmed-meshheading:11217940-Retinal Diseases
,
pubmed-meshheading:11217940-Tomography
,
pubmed-meshheading:11217940-Visual Acuity
,
pubmed-meshheading:11217940-X Chromosome
pubmed:year
2001
pubmed:articleTitle
Optical coherence tomography and electrophysiology in X-linked juvenile retinoschisis associated with a novel mutation in the XLRS1 gene.
pubmed:affiliation
Department of Clinical Ophthalmology, Moorfields Eye Hospital and Institute of Ophthalmology, London, United Kingdom.
pubmed:publicationType
Journal Article
,
Case Reports
,
Research Support, Non-U.S. Gov't