SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
19074810
Source:
http://linkedlifedata.com/resource/pubmed/id/19074810
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:C0012634
,
umls-concept:C0030705
,
umls-concept:C0035298
,
umls-concept:C0271097
,
umls-concept:C0596611
,
umls-concept:C1314792
,
umls-concept:C1417569
pubmed:issue
4
pubmed:dateCreated
2009-3-26
pubmed:abstractText
To study retinal microstructure in Usher Syndrome type 1B (USH1B) caused by MYO7A mutations as a prelude to treatment initiatives.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/7703701
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Myosins
,
http://linkedlifedata.com/resource/pubmed/chemical/myosin VIIa
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1552-5783
pubmed:author
pubmed-author:AlemanTomas STS
,
pubmed-author:CideciyanArtur VAV
,
pubmed-author:JacobsonSamuel GSG
,
pubmed-author:KimberlingWilliam JWJ
,
pubmed-author:RehmHeidi LHL
,
pubmed-author:RomanAlejandro JAJ
,
pubmed-author:SchwartzSharon BSB
,
pubmed-author:SumarokaAlexanderA
,
pubmed-author:WindsorElizabeth A MEA
pubmed:issnType
Electronic
pubmed:volume
50
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1886-94
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:19074810-Adolescent
,
pubmed-meshheading:19074810-Adult
,
pubmed-meshheading:19074810-Child
,
pubmed-meshheading:19074810-Child, Preschool
,
pubmed-meshheading:19074810-Female
,
pubmed-meshheading:19074810-Humans
,
pubmed-meshheading:19074810-Male
,
pubmed-meshheading:19074810-Middle Aged
,
pubmed-meshheading:19074810-Mutation
,
pubmed-meshheading:19074810-Myosins
,
pubmed-meshheading:19074810-Retina
,
pubmed-meshheading:19074810-Retinal Diseases
,
pubmed-meshheading:19074810-Tomography, Optical Coherence
,
pubmed-meshheading:19074810-Usher Syndromes
,
pubmed-meshheading:19074810-Visual Acuity
,
pubmed-meshheading:19074810-Visual Field Tests
,
pubmed-meshheading:19074810-Visual Fields
,
pubmed-meshheading:19074810-Young Adult
pubmed:year
2009
pubmed:articleTitle
Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations.
pubmed:affiliation
Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA. jacobsos@mail.med.upenn.edu
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't