SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
11414642
Source:
http://linkedlifedata.com/resource/pubmed/id/11414642
Search
Subject
(
47
)
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:C0026848
,
umls-concept:C0030705
,
umls-concept:C0935660
,
umls-concept:C1442161
pubmed:issue
2
pubmed:dateCreated
2001-6-20
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/8101187
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Creatine Kinase
,
http://linkedlifedata.com/resource/pubmed/chemical/Glycogen
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0174-304X
pubmed:author
pubmed-author:ArduinoCC
,
pubmed-author:BortolottoSS
,
pubmed-author:BruscoAA
,
pubmed-author:DoriguzziCC
,
pubmed-author:MonginiTT
,
pubmed-author:MutaniRR
,
pubmed-author:PalmucciLL
pubmed:issnType
Print
pubmed:volume
32
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
107-9
pubmed:dateRevised
2008-1-16
pubmed:meshHeading
pubmed-meshheading:11414642-Abnormalities, Multiple
,
pubmed-meshheading:11414642-Adolescent
,
pubmed-meshheading:11414642-Biopsy
,
pubmed-meshheading:11414642-Chromosome Deletion
,
pubmed-meshheading:11414642-Chromosomes, Human, Pair 22
,
pubmed-meshheading:11414642-Craniofacial Abnormalities
,
pubmed-meshheading:11414642-Creatine Kinase
,
pubmed-meshheading:11414642-Glycogen
,
pubmed-meshheading:11414642-Humans
,
pubmed-meshheading:11414642-Male
,
pubmed-meshheading:11414642-Microscopy, Electron
,
pubmed-meshheading:11414642-Muscle, Skeletal
,
pubmed-meshheading:11414642-Muscular Atrophy
,
pubmed-meshheading:11414642-Neuromuscular Diseases
pubmed:year
2001
pubmed:articleTitle
Myopathy in a patient with chromosome 22q11 deletion.
pubmed:publicationType
Letter
,
Case Reports
,
Research Support, Non-U.S. Gov't