16133235

Source:http://linkedlifedata.com/resource/pubmed/id/16133235

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030705, umls-concept:C0039082, umls-concept:C0205191, umls-concept:C0205314, umls-concept:C0205494, umls-concept:C0221912, umls-concept:C0231330, umls-concept:C0521339, umls-concept:C0679622, umls-concept:C1556094
pubmed:issue	12
pubmed:dateCreated	2005-11-14
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7603873
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/NLRP3 protein, human
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0340-6199
pubmed:author	pubmed-author:FurueMasutakaM, pubmed-author:HaraToshiroT, pubmed-author:HayashiMikikoM, pubmed-author:KusuharaKoichiK, pubmed-author:NomuraAkihikoA, pubmed-author:OhgaShouichiS, pubmed-author:TakadaHidetoshiH
pubmed:issnType	Print
pubmed:volume	164
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	785-6
pubmed:dateRevised	2007-7-24
pubmed:meshHeading	pubmed-meshheading:16133235-Asian Continental Ancestry Group, pubmed-meshheading:16133235-Carrier Proteins, pubmed-meshheading:16133235-Craniofacial Abnormalities, pubmed-meshheading:16133235-Female, pubmed-meshheading:16133235-Humans, pubmed-meshheading:16133235-Infant, pubmed-meshheading:16133235-Mutation, pubmed-meshheading:16133235-Neurocutaneous Syndromes, pubmed-meshheading:16133235-Skin
pubmed:year	2005
pubmed:articleTitle	A novel CIAS1mutation in a Japanese patient with chronic infantile neurological cutaneous and articular syndrome.
pubmed:affiliation	Department of Paediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan. takadah@pediatr.med.kyushu-u.ac.jp
pubmed:publicationType	Journal Article, Case Reports