19783878

Source:http://linkedlifedata.com/resource/pubmed/id/19783878

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0018591, umls-concept:C0019202, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0936012, umls-concept:C1412689, umls-concept:C1556095
pubmed:issue	3
pubmed:dateCreated	2009-9-28
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/19783878-19783880
pubmed:language	kor
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101211947
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphatases, http://linkedlifedata.com/resource/pubmed/chemical/Cation Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Wilson disease protein
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	1738-222X
pubmed:author	pubmed-author:JinHyun SeokHS, pubmed-author:OhBermseokB
pubmed:issnType	Print
pubmed:volume	15
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	295-8
pubmed:meshHeading	pubmed-meshheading:19783878-Adenosine Triphosphatases, pubmed-meshheading:19783878-Amino Acid Substitution, pubmed-meshheading:19783878-Cation Transport Proteins, pubmed-meshheading:19783878-Genotype, pubmed-meshheading:19783878-Haplotypes, pubmed-meshheading:19783878-Hepatolenticular Degeneration, pubmed-meshheading:19783878-Humans, pubmed-meshheading:19783878-Mutation, pubmed-meshheading:19783878-Republic of Korea
pubmed:year	2009
pubmed:articleTitle	[Haplotype analysis at R778L mutation of ATP7B gene in Korean patients with Wilson disease].
pubmed:publicationType	Editorial, Comment