20609202

Source:http://linkedlifedata.com/resource/pubmed/id/20609202

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0020792, umls-concept:C0026882, umls-concept:C0205314, umls-concept:C0679622, umls-concept:C1285572, umls-concept:C1285573, umls-concept:C1314763, umls-concept:C1416625, umls-concept:C1524003, umls-concept:C1882417
pubmed:issue	3
pubmed:dateCreated	2010-7-8
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0417360
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Kell Blood-Group System
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1537-2995
pubmed:author	pubmed-author:BordinJosé OJO, pubmed-author:Boturão-NetoEdmirE, pubmed-author:ChibaAkemi KAK
pubmed:issnType	Electronic
pubmed:volume	50
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	735-7
pubmed:meshHeading	pubmed-meshheading:20609202-Brazil, pubmed-meshheading:20609202-Female, pubmed-meshheading:20609202-Genotype, pubmed-meshheading:20609202-Humans, pubmed-meshheading:20609202-Kell Blood-Group System, pubmed-meshheading:20609202-Male, pubmed-meshheading:20609202-Mutation, Missense, pubmed-meshheading:20609202-Polymorphism, Restriction Fragment Length
pubmed:year	2010
pubmed:articleTitle	Novel IVS6-13C>T mutation recognized as a cause of discrepancy between phenotyping and genotyping in KEL*3,4 polymorphism identification.
pubmed:publicationType	Letter