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15653965
Source:
http://linkedlifedata.com/resource/pubmed/id/15653965
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0017431
,
umls-concept:C0031437
,
umls-concept:C0034975
,
umls-concept:C0205246
,
umls-concept:C1275808
,
umls-concept:C1511726
,
umls-concept:C1556084
pubmed:issue
1
pubmed:dateCreated
2005-1-17
pubmed:abstractText
To analyze the main clinical features, genetic mutations, and outcomes of patients of the French Congenital Central Hypoventilation Syndrome (CCHS) Registry.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0231335
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/NBPhox protein
,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0012-3692
pubmed:author
pubmed-author:AmielJeanneJ
,
pubmed-author:BeaufilsFrançoisF
,
pubmed-author:DehanMichelM
,
pubmed-author:French CCHS Working Group
,
pubmed-author:GaultierClaudeC
,
pubmed-author:TrangHaH
,
pubmed-author:ZaccariaIsabelleI
pubmed:issnType
Print
pubmed:volume
127
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
72-9
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15653965-Female
,
pubmed-meshheading:15653965-France
,
pubmed-meshheading:15653965-Genotype
,
pubmed-meshheading:15653965-Hirschsprung Disease
,
pubmed-meshheading:15653965-Homeodomain Proteins
,
pubmed-meshheading:15653965-Humans
,
pubmed-meshheading:15653965-Incidence
,
pubmed-meshheading:15653965-Male
,
pubmed-meshheading:15653965-Mutation
,
pubmed-meshheading:15653965-Phenotype
,
pubmed-meshheading:15653965-Registries
,
pubmed-meshheading:15653965-Sleep Apnea, Central
,
pubmed-meshheading:15653965-Transcription Factors
pubmed:year
2005
pubmed:articleTitle
The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype.
pubmed:affiliation
Service de Physiologie, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Université Paris 7, Paris, France. ha.trang@rdb.ap-hop-paris.fr
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't