| pubmed-article:15766383 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15766383 | lifeskim:mentions | umls-concept:C0012634 | lld:lifeskim |
| pubmed-article:15766383 | lifeskim:mentions | umls-concept:C1519249 | lld:lifeskim |
| pubmed-article:15766383 | lifeskim:mentions | umls-concept:C2717881 | lld:lifeskim |
| pubmed-article:15766383 | lifeskim:mentions | umls-concept:C1705938 | lld:lifeskim |
| pubmed-article:15766383 | lifeskim:mentions | umls-concept:C1527178 | lld:lifeskim |
| pubmed-article:15766383 | pubmed:dateCreated | 2005-4-7 | lld:pubmed |
| pubmed-article:15766383 | pubmed:abstractText | Regions of interest identified through genetic linkage studies regularly exceed 30 centimorgans in size and can contain hundreds of genes. Traditionally this number is reduced by matching functional annotation to knowledge of the disease or phenotype in question. However, here we show that disease genes share patterns of sequence-based features that can provide a good basis for automatic prioritization of candidates by machine learning. | lld:pubmed |
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| pubmed-article:15766383 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15766383 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15766383 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15766383 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15766383 | pubmed:issn | 1471-2105 | lld:pubmed |
| pubmed-article:15766383 | pubmed:author | pubmed-author:PorteousDavid... | lld:pubmed |
| pubmed-article:15766383 | pubmed:author | pubmed-author:EvansKathryn... | lld:pubmed |
| pubmed-article:15766383 | pubmed:author | pubmed-author:AdamsRichard... | lld:pubmed |
| pubmed-article:15766383 | pubmed:author | pubmed-author:PickardBen... | lld:pubmed |
| pubmed-article:15766383 | pubmed:author | pubmed-author:AdieEuan AEA | lld:pubmed |
| pubmed-article:15766383 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:15766383 | pubmed:volume | 6 | lld:pubmed |
| pubmed-article:15766383 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15766383 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15766383 | pubmed:pagination | 55 | lld:pubmed |
| pubmed-article:15766383 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:15766383 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15766383 | pubmed:articleTitle | Speeding disease gene discovery by sequence based candidate prioritization. | lld:pubmed |
| pubmed-article:15766383 | pubmed:affiliation | Medical Genetics Section, Department of Medical Sciences, The University of Edinburgh, Edinburgh, UK. euan.adie@ed.ac.uk | lld:pubmed |
| pubmed-article:15766383 | pubmed:publicationType | Journal Article | lld:pubmed |
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