SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
19159393
Source:
http://linkedlifedata.com/resource/pubmed/id/19159393
Search
Subject
(
49
)
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:C0030705
,
umls-concept:C0205210
,
umls-concept:C0265354
,
umls-concept:C0796344
,
umls-concept:C1427038
,
umls-concept:C1556095
pubmed:issue
3
pubmed:dateCreated
2009-3-4
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0253664
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CHD7 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Helicases
,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1399-0004
pubmed:author
pubmed-author:ChaKK
,
pubmed-author:HongH SHS
,
pubmed-author:KimJ-WJW
,
pubmed-author:LeeY KYK
,
pubmed-author:LeeY-WYW
,
pubmed-author:MOER HRH
,
pubmed-author:ShimY MYM
pubmed:issnType
Electronic
pubmed:volume
75
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
290-3
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:19159393-Abnormalities, Multiple
,
pubmed-meshheading:19159393-Base Sequence
,
pubmed-meshheading:19159393-Child, Preschool
,
pubmed-meshheading:19159393-DNA Helicases
,
pubmed-meshheading:19159393-DNA Mutational Analysis
,
pubmed-meshheading:19159393-DNA-Binding Proteins
,
pubmed-meshheading:19159393-Female
,
pubmed-meshheading:19159393-Heart Defects, Congenital
,
pubmed-meshheading:19159393-Humans
,
pubmed-meshheading:19159393-Intellectual Disability
,
pubmed-meshheading:19159393-Korea
,
pubmed-meshheading:19159393-Male
,
pubmed-meshheading:19159393-Molecular Sequence Data
,
pubmed-meshheading:19159393-Syndrome
pubmed:year
2009
pubmed:articleTitle
Clinical and genetic analysis of the CHD7 gene in Korean patients with CHARGE syndrome.
pubmed:publicationType
Letter
,
Case Reports