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10974341
Source:
http://linkedlifedata.com/resource/pubmed/id/10974341
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0017337
,
umls-concept:C0205341
,
umls-concept:C0907532
,
umls-concept:C1861172
,
umls-concept:C1882417
pubmed:issue
6
pubmed:dateCreated
2000-12-7
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0326377
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Factor V
,
http://linkedlifedata.com/resource/pubmed/chemical/NOS3 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase
,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type III
,
http://linkedlifedata.com/resource/pubmed/chemical/Prothrombin
,
http://linkedlifedata.com/resource/pubmed/chemical/factor V Leiden
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0049-3848
pubmed:author
pubmed-author:AlvarezM VMV
,
pubmed-author:CarreiraJ MJM
,
pubmed-author:FrancoA GAG
,
pubmed-author:GarcíaE CEC
,
pubmed-author:OrdóñezA JAJ
,
pubmed-author:SánchezL MLM
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
99
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
563-6
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:10974341-Adult
,
pubmed-meshheading:10974341-Age of Onset
,
pubmed-meshheading:10974341-Aged
,
pubmed-meshheading:10974341-Aged, 80 and over
,
pubmed-meshheading:10974341-European Continental Ancestry Group
,
pubmed-meshheading:10974341-Factor V
,
pubmed-meshheading:10974341-Female
,
pubmed-meshheading:10974341-Gene Frequency
,
pubmed-meshheading:10974341-Genetic Predisposition to Disease
,
pubmed-meshheading:10974341-Genotype
,
pubmed-meshheading:10974341-Humans
,
pubmed-meshheading:10974341-Introns
,
pubmed-meshheading:10974341-Male
,
pubmed-meshheading:10974341-Middle Aged
,
pubmed-meshheading:10974341-Nitric Oxide Synthase
,
pubmed-meshheading:10974341-Nitric Oxide Synthase Type III
,
pubmed-meshheading:10974341-Point Mutation
,
pubmed-meshheading:10974341-Polymorphism, Genetic
,
pubmed-meshheading:10974341-Prevalence
,
pubmed-meshheading:10974341-Prothrombin
,
pubmed-meshheading:10974341-Spain
,
pubmed-meshheading:10974341-Tandem Repeat Sequences
,
pubmed-meshheading:10974341-Thromboembolism
,
pubmed-meshheading:10974341-Venous Thrombosis
pubmed:year
2000
pubmed:articleTitle
Two expressive polymorphisms on the endothelial nitric oxide synthase gene (intron4, 27 bp repeat and -786 T/C) and the venous thromboembolism.
pubmed:affiliation
Hematology Department, Oviedo, Spain. jagonzalez@medynet.com
pubmed:publicationType
Journal Article
,
Comparative Study