18568368

Source:http://linkedlifedata.com/resource/pubmed/id/18568368

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0034897, umls-concept:C0206042, umls-concept:C1704711, umls-concept:C2348867
pubmed:issue	4
pubmed:dateCreated	2008-9-26
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/Z01 NS002973-09
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/18568368-12205650, http://linkedlifedata.com/resource/pubmed/commentcorrection/18568368-18347820
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9709714
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/PRNP protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Prions
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1364-6753
pubmed:author	pubmed-author:GoldfarbL GLG, pubmed-author:KUHJ RJR
pubmed:issnType	Electronic
pubmed:volume	9
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	301-2; author reply 303-4
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:18568368-Female, pubmed-meshheading:18568368-Founder Effect, pubmed-meshheading:18568368-Gene Frequency, pubmed-meshheading:18568368-Haplotypes, pubmed-meshheading:18568368-Humans, pubmed-meshheading:18568368-Insomnia, Fatal Familial, pubmed-meshheading:18568368-Male, pubmed-meshheading:18568368-Mutation, Missense, pubmed-meshheading:18568368-Polymorphism, Single Nucleotide, pubmed-meshheading:18568368-Prions
pubmed:year	2008
pubmed:articleTitle	Global distribution of fatal familial insomnia: founder or recurrent mutations.
pubmed:publicationType	Letter, Comment