SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
4646548
Source:
http://linkedlifedata.com/resource/pubmed/id/4646548
Search
Subject
(
57
)
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:C0000768
,
umls-concept:C0008633
,
umls-concept:C0011155
,
umls-concept:C0237401
,
umls-concept:C0332597
,
umls-concept:C0424972
,
umls-concept:C0678227
,
umls-concept:C1522538
pubmed:issue
4
pubmed:dateCreated
1973-3-8
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/4646548-13989383
,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4646548-14042837
,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4646548-14148233
,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4646548-4097524
,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4646548-4104181
,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4646548-5106368
,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4646548-5619932
,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4646548-5970335
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Blood Group Antigens
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0022-2593
pubmed:author
pubmed-author:HalldórssonSS
,
pubmed-author:HauksdóttirHH
,
pubmed-author:JenssonOO
,
pubmed-author:McDermottAA
,
pubmed-author:MikkelsenMM
pubmed:issnType
Print
pubmed:volume
9
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
413-21
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:4646548-Abnormalities, Multiple
,
pubmed-meshheading:4646548-Blood Group Antigens
,
pubmed-meshheading:4646548-Child, Preschool
,
pubmed-meshheading:4646548-Chromosome Aberrations
,
pubmed-meshheading:4646548-Chromosomes, Human, 13-15
,
pubmed-meshheading:4646548-Crossing Over, Genetic
,
pubmed-meshheading:4646548-Facial Expression
,
pubmed-meshheading:4646548-Female
,
pubmed-meshheading:4646548-Genitalia
,
pubmed-meshheading:4646548-Growth Disorders
,
pubmed-meshheading:4646548-Humans
,
pubmed-meshheading:4646548-Intellectual Disability
,
pubmed-meshheading:4646548-Karyotyping
,
pubmed-meshheading:4646548-Male
,
pubmed-meshheading:4646548-Meiosis
,
pubmed-meshheading:4646548-Pedigree
,
pubmed-meshheading:4646548-Phenotype
pubmed:year
1972
pubmed:articleTitle
Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals.
pubmed:publicationType
Journal Article