12687678

Source:http://linkedlifedata.com/resource/pubmed/id/12687678

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0032659, umls-concept:C0376249, umls-concept:C1417925, umls-concept:C1556094
pubmed:issue	4
pubmed:dateCreated	2003-4-10
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/OCA2 protein, human
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	1552-4825
pubmed:author	pubmed-author:MiyamuraYoshinoriY, pubmed-author:SuzukiTamioT, pubmed-author:TomitaYasushiY
pubmed:issnType	Print
pubmed:day	1
pubmed:volume	118A
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	402-3
pubmed:dateRevised	2008-5-21
pubmed:meshHeading	pubmed-meshheading:12687678-Albinism, Oculocutaneous, pubmed-meshheading:12687678-Carrier Proteins, pubmed-meshheading:12687678-Humans, pubmed-meshheading:12687678-Japan, pubmed-meshheading:12687678-Membrane Proteins, pubmed-meshheading:12687678-Membrane Transport Proteins, pubmed-meshheading:12687678-Mutation, Missense, pubmed-meshheading:12687678-Polymorphism, Single-Stranded Conformational
pubmed:year	2003
pubmed:articleTitle	High frequency of the Ala481Thr mutation of the P gene in the Japanese population.
pubmed:publicationType	Letter, Comparative Study, Research Support, Non-U.S. Gov't