SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
1338761
Source:
http://linkedlifedata.com/resource/pubmed/id/1338761
Search
Subject
(
44
)
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:C0027126
,
umls-concept:C0179630
,
umls-concept:C0205341
,
umls-concept:C0332281
,
umls-concept:C0441587
,
umls-concept:C1442161
,
umls-concept:C1705968
,
umls-concept:C1882417
pubmed:issue
6
pubmed:dateCreated
1993-6-7
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9208958
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA Transposable Elements
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0964-6906
pubmed:author
pubmed-author:BrookJ DJD
,
pubmed-author:CrowS RSR
,
pubmed-author:HarleyH GHG
,
pubmed-author:RundleS ASA
,
pubmed-author:ShawD JDJ
pubmed:issnType
Print
pubmed:volume
1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
451
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:1338761-Base Sequence
,
pubmed-meshheading:1338761-Chromosome Banding
,
pubmed-meshheading:1338761-Chromosome Mapping
,
pubmed-meshheading:1338761-Chromosomes, Human, Pair 19
,
pubmed-meshheading:1338761-DNA Transposable Elements
,
pubmed-meshheading:1338761-Humans
,
pubmed-meshheading:1338761-Myotonic Dystrophy
,
pubmed-meshheading:1338761-Polymorphism, Genetic
,
pubmed-meshheading:1338761-Repetitive Sequences, Nucleic Acid
,
pubmed-meshheading:1338761-Sequence Deletion
pubmed:year
1992
pubmed:articleTitle
Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat.
pubmed:affiliation
Institute of Medical Genetics, University of Wales College of Medicine, Heath Park, Cardiff, UK.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't