SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
17768376
Source:
http://linkedlifedata.com/resource/pubmed/id/17768376
Search
Subject
(
55
)
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:C0015576
,
umls-concept:C0026882
,
umls-concept:C0028738
,
umls-concept:C0152035
,
umls-concept:C0241764
,
umls-concept:C1513492
,
umls-concept:C1705994
,
umls-concept:C1744681
,
umls-concept:C1825315
pubmed:dateCreated
2007-9-4
pubmed:abstractText
To identify mutations causing X-linked congenital motor nystagmus (XL-CMN) in Chinese families.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9605351
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Cytoskeletal Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/FRMD7 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins
pubmed:status
MEDLINE
pubmed:issn
1090-0535
pubmed:author
pubmed-author:GuoXiangmingX
,
pubmed-author:LiShiqiangS
,
pubmed-author:XiaoXueshanX
,
pubmed-author:ZhangQingjiongQ
pubmed:issnType
Electronic
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1375-8
pubmed:meshHeading
pubmed-meshheading:17768376-Adolescent
,
pubmed-meshheading:17768376-Adult
,
pubmed-meshheading:17768376-Aged
,
pubmed-meshheading:17768376-Aged, 80 and over
,
pubmed-meshheading:17768376-Asian Continental Ancestry Group
,
pubmed-meshheading:17768376-Base Sequence
,
pubmed-meshheading:17768376-Child
,
pubmed-meshheading:17768376-Child, Preschool
,
pubmed-meshheading:17768376-China
,
pubmed-meshheading:17768376-Cytoskeletal Proteins
,
pubmed-meshheading:17768376-DNA Mutational Analysis
,
pubmed-meshheading:17768376-Female
,
pubmed-meshheading:17768376-Genetic Diseases, X-Linked
,
pubmed-meshheading:17768376-Humans
,
pubmed-meshheading:17768376-Male
,
pubmed-meshheading:17768376-Membrane Proteins
,
pubmed-meshheading:17768376-Middle Aged
,
pubmed-meshheading:17768376-Molecular Sequence Data
,
pubmed-meshheading:17768376-Mutation
,
pubmed-meshheading:17768376-Nystagmus, Congenital
,
pubmed-meshheading:17768376-Pedigree
pubmed:year
2007
pubmed:articleTitle
FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus.
pubmed:affiliation
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China. qingjiongzhang@yahoo.com
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't