SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
4698934
Source:
http://linkedlifedata.com/resource/pubmed/id/4698934
Search
Subject
(
60
)
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:C0013336
,
umls-concept:C0020758
,
umls-concept:C0039082
,
umls-concept:C0333641
,
umls-concept:C1847868
,
umls-concept:C1880022
,
umls-concept:C1970780
pubmed:issue
3
pubmed:dateCreated
1973-6-21
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0375410
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Uric Acid
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0022-3476
pubmed:author
pubmed-author:Bat-MiriamMM
,
pubmed-author:CohenB EBE
,
pubmed-author:CrispinMM
,
pubmed-author:GoodmanRR
,
pubmed-author:KatznelsonDD
,
pubmed-author:PasswellJJ
,
pubmed-author:PollakSS
,
pubmed-author:SzeinbergAA
,
pubmed-author:ZipperkowskiLL
pubmed:issnType
Print
pubmed:volume
82
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
466-71
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:4698934-Adolescent
,
pubmed-meshheading:4698934-Amino Acid Metabolism, Inborn Errors
,
pubmed-meshheading:4698934-Atrophy
,
pubmed-meshheading:4698934-Biopsy
,
pubmed-meshheading:4698934-Child
,
pubmed-meshheading:4698934-Consanguinity
,
pubmed-meshheading:4698934-Dermatoglyphics
,
pubmed-meshheading:4698934-Dwarfism
,
pubmed-meshheading:4698934-Female
,
pubmed-meshheading:4698934-Glucose Tolerance Test
,
pubmed-meshheading:4698934-Glycosuria, Renal
,
pubmed-meshheading:4698934-Humans
,
pubmed-meshheading:4698934-Hypergammaglobulinemia
,
pubmed-meshheading:4698934-Ichthyosis
,
pubmed-meshheading:4698934-Intellectual Disability
,
pubmed-meshheading:4698934-Male
,
pubmed-meshheading:4698934-Nails, Malformed
,
pubmed-meshheading:4698934-Oral Manifestations
,
pubmed-meshheading:4698934-Pedigree
,
pubmed-meshheading:4698934-Renal Tubular Transport, Inborn Errors
,
pubmed-meshheading:4698934-Skin
,
pubmed-meshheading:4698934-Skin Diseases
,
pubmed-meshheading:4698934-Syndrome
,
pubmed-meshheading:4698934-Tooth Abnormalities
,
pubmed-meshheading:4698934-Uric Acid
pubmed:year
1973
pubmed:articleTitle
A syndrome characterized by congenital ichthyosis with atrophy, mental retardation, dwarfism, and generalized aminoaciduria.
pubmed:publicationType
Journal Article