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16824815
Source:
http://linkedlifedata.com/resource/pubmed/id/16824815
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53
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0205214
,
umls-concept:C0314603
,
umls-concept:C0332120
,
umls-concept:C0406709
,
umls-concept:C1314792
,
umls-concept:C1785148
pubmed:issue
6
pubmed:dateCreated
2006-12-20
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/101247089
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/TP63 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators
,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Proteins
pubmed:status
MEDLINE
pubmed:issn
1769-7212
pubmed:author
pubmed-author:BelligniEE
,
pubmed-author:BrunelloGG
,
pubmed-author:CarandoAA
,
pubmed-author:Cirillo SilengoMM
,
pubmed-author:DianzaniII
,
pubmed-author:FerreroG BGB
,
pubmed-author:GarelliEE
,
pubmed-author:MartanoCC
,
pubmed-author:SorasioLL
pubmed:issnType
Print
pubmed:volume
49
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
520-2
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:16824815-Abnormalities, Multiple
,
pubmed-meshheading:16824815-Adult
,
pubmed-meshheading:16824815-Cleft Lip
,
pubmed-meshheading:16824815-Cleft Palate
,
pubmed-meshheading:16824815-DNA-Binding Proteins
,
pubmed-meshheading:16824815-Ectodermal Dysplasia
,
pubmed-meshheading:16824815-Eyelids
,
pubmed-meshheading:16824815-Female
,
pubmed-meshheading:16824815-Humans
,
pubmed-meshheading:16824815-Infant, Newborn
,
pubmed-meshheading:16824815-Male
,
pubmed-meshheading:16824815-Point Mutation
,
pubmed-meshheading:16824815-Syndrome
,
pubmed-meshheading:16824815-Trans-Activators
,
pubmed-meshheading:16824815-Transcription Factors
,
pubmed-meshheading:16824815-Tumor Suppressor Proteins
pubmed:articleTitle
AEC syndrome: further evidence of a common genetic etiology with Rapp-Hodgkin syndrome.
pubmed:publicationType
Letter
,
Case Reports