SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
10777363
Source:
http://linkedlifedata.com/resource/pubmed/id/10777363
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:C0004903
,
umls-concept:C0796357
,
umls-concept:C1332838
,
umls-concept:C1333887
,
umls-concept:C1334091
,
umls-concept:C1417598
pubmed:issue
3
pubmed:dateCreated
2000-4-20
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/H19 long non-coding RNA
,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor II
,
http://linkedlifedata.com/resource/pubmed/chemical/Muscle Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/NAP1L4 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Untranslated
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0022-2593
pubmed:author
pubmed-author:CatchpooleDD
,
pubmed-author:JoyceJ AJA
,
pubmed-author:LamWW
,
pubmed-author:MaherE RER
,
pubmed-author:MunroeDD
,
pubmed-author:MurrellAA
,
pubmed-author:ReidLL
,
pubmed-author:SchofieldP NPN
,
pubmed-author:SmallwoodA VAV
,
pubmed-author:TangTT
pubmed:issnType
Print
pubmed:volume
37
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
212-5
pubmed:dateRevised
2011-10-7
pubmed:meshHeading
pubmed-meshheading:10777363-Beckwith-Wiedemann Syndrome
,
pubmed-meshheading:10777363-DNA Methylation
,
pubmed-meshheading:10777363-DNA Mutational Analysis
,
pubmed-meshheading:10777363-Humans
,
pubmed-meshheading:10777363-Insulin-Like Growth Factor II
,
pubmed-meshheading:10777363-Muscle Proteins
,
pubmed-meshheading:10777363-Nuclear Proteins
,
pubmed-meshheading:10777363-Polymorphism, Genetic
,
pubmed-meshheading:10777363-RNA, Untranslated
pubmed:year
2000
pubmed:articleTitle
Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome.
pubmed:publicationType
Letter