SPARQL
Query
Update
Search
Quick
Advanced
Co-occurrence
RelFinder
About
Sources
Admin
System Info
Repository Management
Search Configuration
Sources
17661761
Source:
http://linkedlifedata.com/resource/pubmed/id/17661761
Search
Subject
(
64
)
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:C0022277
,
umls-concept:C0026882
,
umls-concept:C0032659
,
umls-concept:C0205099
,
umls-concept:C0205164
,
umls-concept:C0700164
,
umls-concept:C1384665
,
umls-concept:C1518029
,
umls-concept:C2348164
pubmed:issue
4
pubmed:dateCreated
2007-7-30
pubmed:abstractText
The C282Y mutation in the HFE gene is responsible for most cases of hereditary haemochromatosis.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/8707234
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/HFE protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class I
,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0269-2813
pubmed:author
pubmed-author:BaldoVV
,
pubmed-author:BassoDD
,
pubmed-author:ChiaramonteMM
,
pubmed-author:DI AndreaOO
,
pubmed-author:FloreaniAA
,
pubmed-author:MarraMM
,
pubmed-author:NavagliaFF
,
pubmed-author:PetridisII
,
pubmed-author:Rosa RizzottoEE
,
pubmed-author:TestaRR
,
pubmed-author:ZaninottoMM
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
26
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
577-86
pubmed:meshHeading
pubmed-meshheading:17661761-Adolescent
,
pubmed-meshheading:17661761-Adult
,
pubmed-meshheading:17661761-Aged
,
pubmed-meshheading:17661761-Aged, 80 and over
,
pubmed-meshheading:17661761-Child
,
pubmed-meshheading:17661761-Female
,
pubmed-meshheading:17661761-Gene Expression
,
pubmed-meshheading:17661761-Gene Frequency
,
pubmed-meshheading:17661761-Hemochromatosis
,
pubmed-meshheading:17661761-Histocompatibility Antigens Class I
,
pubmed-meshheading:17661761-Humans
,
pubmed-meshheading:17661761-Iron Overload
,
pubmed-meshheading:17661761-Italy
,
pubmed-meshheading:17661761-Liver Diseases
,
pubmed-meshheading:17661761-Male
,
pubmed-meshheading:17661761-Membrane Proteins
,
pubmed-meshheading:17661761-Middle Aged
,
pubmed-meshheading:17661761-Mutation
,
pubmed-meshheading:17661761-Population Surveillance
,
pubmed-meshheading:17661761-Prevalence
pubmed:year
2007
pubmed:articleTitle
An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy.
pubmed:affiliation
Department of Surgical and Gastroenterological Sciences, University of Padu, Via Giustiniani 2, 35128 Padua, Italy. annarosa.floreani@unipd.it
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't