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17343268
Source:
http://linkedlifedata.com/resource/pubmed/id/17343268
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0037047
,
umls-concept:C0441748
,
umls-concept:C1332838
,
umls-concept:C1412805
,
umls-concept:C1417943
,
umls-concept:C1857345
,
umls-concept:C2828389
pubmed:issue
7
pubmed:dateCreated
2007-3-27
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/BMP4 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Bone Morphogenetic Protein 4
,
http://linkedlifedata.com/resource/pubmed/chemical/Bone Morphogenetic Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Ketoglutarate Dehydrogenase Complex
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1552-4825
pubmed:author
pubmed-author:BalemansWendyW
,
pubmed-author:CourtensWinnieW
,
pubmed-author:DuvalEls L I MEL
,
pubmed-author:EyskensFrançoisF
,
pubmed-author:JespersAnnA
,
pubmed-author:van BeverYolandeY
,
pubmed-author:van HulWimW
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
143
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
763-7
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:17343268-Bone Morphogenetic Protein 4
,
pubmed-meshheading:17343268-Bone Morphogenetic Proteins
,
pubmed-meshheading:17343268-Deafness
,
pubmed-meshheading:17343268-Female
,
pubmed-meshheading:17343268-Foot Bones
,
pubmed-meshheading:17343268-Genes, Recessive
,
pubmed-meshheading:17343268-Hand Bones
,
pubmed-meshheading:17343268-Humans
,
pubmed-meshheading:17343268-Infant
,
pubmed-meshheading:17343268-Infant, Newborn
,
pubmed-meshheading:17343268-Ketoglutarate Dehydrogenase Complex
,
pubmed-meshheading:17343268-Male
,
pubmed-meshheading:17343268-Pedigree
,
pubmed-meshheading:17343268-Siblings
,
pubmed-meshheading:17343268-Syndrome
pubmed:year
2007
pubmed:articleTitle
Exclusion of OGDH and BMP4 as candidate genes in two siblings with autosomal recessive DOOR syndrome.
pubmed:affiliation
Department of Medical Genetics, University Hospital Antwerp, Edegem, Belgium. y.vanbever@erasmusmn.nl
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't