SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
15164414
Source:
http://linkedlifedata.com/resource/pubmed/id/15164414
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:C0033053
,
umls-concept:C0243067
,
umls-concept:C0314603
,
umls-concept:C0449445
,
umls-concept:C0597619
pubmed:issue
5
pubmed:dateCreated
2004-5-27
pubmed:abstractText
To demonstrate the feasibility of prenatal diagnosis by molecular genetics in all urea cycle defects in order to improve and standardize the current approaches.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/8106540
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Acetyltransferases
,
http://linkedlifedata.com/resource/pubmed/chemical/Amino-Acid N-Acetyltransferase
,
http://linkedlifedata.com/resource/pubmed/chemical/Argininosuccinate Synthase
,
http://linkedlifedata.com/resource/pubmed/chemical/Carbamoyl-Phosphate Synthase...
,
http://linkedlifedata.com/resource/pubmed/chemical/NAGS protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Urea
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0197-3851
pubmed:author
pubmed-author:HäberleJohannesJ
,
pubmed-author:KochHans GeorgHG
pubmed:copyrightInfo
Copyright 2004 John Wiley & Sons, Ltd.
pubmed:issnType
Print
pubmed:volume
24
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
378-83
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:15164414-Acetyltransferases
,
pubmed-meshheading:15164414-Amino-Acid N-Acetyltransferase
,
pubmed-meshheading:15164414-Argininosuccinate Synthase
,
pubmed-meshheading:15164414-Argininosuccinic Aciduria
,
pubmed-meshheading:15164414-Carbamoyl-Phosphate Synthase (Ammonia)
,
pubmed-meshheading:15164414-Chorionic Villi Sampling
,
pubmed-meshheading:15164414-Female
,
pubmed-meshheading:15164414-Genetic Testing
,
pubmed-meshheading:15164414-Humans
,
pubmed-meshheading:15164414-Hyperargininemia
,
pubmed-meshheading:15164414-Metabolism, Inborn Errors
,
pubmed-meshheading:15164414-Ornithine Carbamoyltransferase Deficiency Disease
,
pubmed-meshheading:15164414-Pregnancy
,
pubmed-meshheading:15164414-Prenatal Diagnosis
,
pubmed-meshheading:15164414-Urea
pubmed:year
2004
pubmed:articleTitle
Genetic approach to prenatal diagnosis in urea cycle defects.
pubmed:affiliation
Universitätsklinikum Münster, Klinik und Poliklinik für Kinderheilkunde, Münster, Germany. haeb@uni-muenster.de
pubmed:publicationType
Journal Article