17657198

Source:http://linkedlifedata.com/resource/pubmed/id/17657198

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0009219, umls-concept:C0013575, umls-concept:C0017342, umls-concept:C0026882, umls-concept:C0343111, umls-concept:C0406778, umls-concept:C0439849, umls-concept:C0445223, umls-concept:C0669391, umls-concept:C1416717, umls-concept:C1552599, umls-concept:C1704787
pubmed:issue	6-7
pubmed:dateCreated	2007-7-27
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7702013
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Codon, Nonsense, http://linkedlifedata.com/resource/pubmed/chemical/Keratin-14
pubmed:status	MEDLINE
pubmed:issn	0151-9638
pubmed:author	pubmed-author:DereureOO
pubmed:issnType	Print
pubmed:volume	134
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	595
pubmed:meshHeading	pubmed-meshheading:17657198-Codon, Nonsense, pubmed-meshheading:17657198-Ectodermal Dysplasia, pubmed-meshheading:17657198-Genes, Dominant, pubmed-meshheading:17657198-Humans, pubmed-meshheading:17657198-Hyperpigmentation, pubmed-meshheading:17657198-Keratin-14, pubmed-meshheading:17657198-Keratoderma, Palmoplantar, pubmed-meshheading:17657198-Phenotype, pubmed-meshheading:17657198-Syndrome, pubmed-meshheading:17657198-Tooth Abnormalities
pubmed:articleTitle	[Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis. Two allelic ectodermal dysplasias related to mutations of dominant gene coding for keratin 14].
pubmed:affiliation	Service de Dermatologie, Hôpital Saint Eloi, 80, avenue Augustin Fliche, 34295 Montpellier Cedex 5. o-dereure@chu-montpellier.fr
pubmed:publicationType	Journal Article