18348274

Source:http://linkedlifedata.com/resource/pubmed/id/18348274

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0043008, umls-concept:C0086409, umls-concept:C0205422, umls-concept:C0332307, umls-concept:C0599155, umls-concept:C0679058, umls-concept:C1515568, umls-concept:C1533148, umls-concept:C1547699, umls-concept:C1571654, umls-concept:C2700640
pubmed:issue	8
pubmed:dateCreated	2008-4-2
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/High Mobility Group Proteins, http://linkedlifedata.com/resource/pubmed/chemical/SOX10 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/SOXE Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1552-4833
pubmed:author	pubmed-author:MorínMatíasM, pubmed-author:Moreno-PelayoMiguel AMA, pubmed-author:MorenoFelipeF, pubmed-author:RiveraTeresaT, pubmed-author:ViñuelaAntonioA, pubmed-author:VillamarManuelaM, pubmed-author:del CastilloIgnacioI
pubmed:issnType	Electronic
pubmed:day	15
pubmed:volume	146A
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1032-7
pubmed:dateRevised	2008-11-21
pubmed:meshHeading	pubmed-meshheading:18348274-DNA-Binding Proteins, pubmed-meshheading:18348274-Hearing Loss, Sensorineural, pubmed-meshheading:18348274-High Mobility Group Proteins, pubmed-meshheading:18348274-Humans, pubmed-meshheading:18348274-Infant, pubmed-meshheading:18348274-Male, pubmed-meshheading:18348274-Mutation, Missense, pubmed-meshheading:18348274-SOXE Transcription Factors, pubmed-meshheading:18348274-Spain, pubmed-meshheading:18348274-Transcription Factors, pubmed-meshheading:18348274-Waardenburg's Syndrome
pubmed:year	2008
pubmed:articleTitle	A de novo missense mutation in the gene encoding the SOX10 transcription factor in a Spanish sporadic case of Waardenburg syndrome type IV.
pubmed:affiliation	Unidad de Genética Molecular, Hospital Universitario Ramón y Cajal, Madrid, Spain.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't