SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
18247312
Source:
http://linkedlifedata.com/resource/pubmed/id/18247312
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:C0019569
,
umls-concept:C0162735
,
umls-concept:C0796451
,
umls-concept:C1420069
pubmed:issue
1
pubmed:dateCreated
2008-2-5
pubmed:abstractText
To investigate the point mutations and polymorphisms of SIP1 gene in Hirschsprung disease(HSCR) and discuss the relationship between the feature of gene mutations and single nucleotide polymorphisms of SIP1 gene and HSCR.
pubmed:language
chi
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9425197
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/GEMIN2 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1003-9406
pubmed:author
pubmed-author:GaoHongH
,
pubmed-author:HuangYingY
,
pubmed-author:LiXin-fangXF
,
pubmed-author:WangWei-linWL
,
pubmed-author:ZhangZhi-boZB
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
82-5
pubmed:dateRevised
2011-9-28
pubmed:meshHeading
pubmed-meshheading:18247312-Adolescent
,
pubmed-meshheading:18247312-Base Sequence
,
pubmed-meshheading:18247312-Child
,
pubmed-meshheading:18247312-Child, Preschool
,
pubmed-meshheading:18247312-DNA Mutational Analysis
,
pubmed-meshheading:18247312-Exons
,
pubmed-meshheading:18247312-Female
,
pubmed-meshheading:18247312-Hirschsprung Disease
,
pubmed-meshheading:18247312-Humans
,
pubmed-meshheading:18247312-Male
,
pubmed-meshheading:18247312-Molecular Sequence Data
,
pubmed-meshheading:18247312-Nerve Tissue Proteins
,
pubmed-meshheading:18247312-Point Mutation
,
pubmed-meshheading:18247312-Polymerase Chain Reaction
,
pubmed-meshheading:18247312-Polymorphism, Single Nucleotide
,
pubmed-meshheading:18247312-Polymorphism, Single-Stranded Conformational
,
pubmed-meshheading:18247312-RNA-Binding Proteins
pubmed:year
2008
pubmed:articleTitle
[Coding-sequence point mutation and polymorphism analyses of SIP1 gene in Hirschsprung disease].
pubmed:affiliation
Shengjing Affiliated Hospital, China Medical University, Shenyang, Liaoning, 110004 People's Republic of China.
pubmed:publicationType
Journal Article
,
English Abstract
,
Research Support, Non-U.S. Gov't