Source:http://linkedlifedata.com/resource/pubmed/id/15900311
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
|
pubmed:dateCreated |
2005-7-25
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
1018-4813
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
13
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
898-901
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:15900311-Alleles,
pubmed-meshheading:15900311-Base Sequence,
pubmed-meshheading:15900311-Computational Biology,
pubmed-meshheading:15900311-Gene Frequency,
pubmed-meshheading:15900311-Genotype,
pubmed-meshheading:15900311-Haplotypes,
pubmed-meshheading:15900311-Phylogeny,
pubmed-meshheading:15900311-Polymorphism, Single Nucleotide
|
pubmed:year |
2005
|
pubmed:articleTitle |
Typing without calling the allele: a strategy for inferring SNP haplotypes.
|
pubmed:publicationType |
Letter,
Research Support, Non-U.S. Gov't
|