10051024

Source:http://linkedlifedata.com/resource/pubmed/id/10051024

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019202, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0337816, umls-concept:C1412689
pubmed:issue	2
pubmed:dateCreated	1999-5-12
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphatases, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cation Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Wilson disease protein
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0022-2593
pubmed:author	pubmed-author:DeinekoN LNL, pubmed-author:IllarioshkinS NSN, pubmed-author:Ivanova-SmolenskayaI AIA, pubmed-author:KarabanovA VAV, pubmed-author:MarkovaE DED, pubmed-author:OvchinnikovI VIV, pubmed-author:PoleshchukV VVV
pubmed:issnType	Print
pubmed:volume	36
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	174
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:10051024-Adenosine Triphosphatases, pubmed-meshheading:10051024-Carrier Proteins, pubmed-meshheading:10051024-Cation Transport Proteins, pubmed-meshheading:10051024-Chromosomes, Human, Pair 13, pubmed-meshheading:10051024-Hepatolenticular Degeneration, pubmed-meshheading:10051024-Humans, pubmed-meshheading:10051024-Point Mutation, pubmed-meshheading:10051024-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:10051024-Russia
pubmed:year	1999
pubmed:articleTitle	The His1069Gln mutation in the ATP7B gene in Russian patients with Wilson disease.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't