| pubmed-article:18247312 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18247312 | lifeskim:mentions | umls-concept:C0019569 | lld:lifeskim |
| pubmed-article:18247312 | lifeskim:mentions | umls-concept:C0162735 | lld:lifeskim |
| pubmed-article:18247312 | lifeskim:mentions | umls-concept:C1420069 | lld:lifeskim |
| pubmed-article:18247312 | lifeskim:mentions | umls-concept:C0796451 | lld:lifeskim |
| pubmed-article:18247312 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:18247312 | pubmed:dateCreated | 2008-2-5 | lld:pubmed |
| pubmed-article:18247312 | pubmed:abstractText | To investigate the point mutations and polymorphisms of SIP1 gene in Hirschsprung disease(HSCR) and discuss the relationship between the feature of gene mutations and single nucleotide polymorphisms of SIP1 gene and HSCR. | lld:pubmed |
| pubmed-article:18247312 | pubmed:language | chi | lld:pubmed |
| pubmed-article:18247312 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18247312 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18247312 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18247312 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18247312 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18247312 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18247312 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:18247312 | pubmed:issn | 1003-9406 | lld:pubmed |
| pubmed-article:18247312 | pubmed:author | pubmed-author:HuangYingY | lld:pubmed |
| pubmed-article:18247312 | pubmed:author | pubmed-author:GaoHongH | lld:pubmed |
| pubmed-article:18247312 | pubmed:author | pubmed-author:WangWei-linWL | lld:pubmed |
| pubmed-article:18247312 | pubmed:author | pubmed-author:ZhangZhi-boZB | lld:pubmed |
| pubmed-article:18247312 | pubmed:author | pubmed-author:LiXin-fangXF | lld:pubmed |
| pubmed-article:18247312 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:18247312 | pubmed:volume | 25 | lld:pubmed |
| pubmed-article:18247312 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18247312 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18247312 | pubmed:pagination | 82-5 | lld:pubmed |
| pubmed-article:18247312 | pubmed:dateRevised | 2011-9-28 | lld:pubmed |
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| pubmed-article:18247312 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18247312 | pubmed:articleTitle | [Coding-sequence point mutation and polymorphism analyses of SIP1 gene in Hirschsprung disease]. | lld:pubmed |
| pubmed-article:18247312 | pubmed:affiliation | Shengjing Affiliated Hospital, China Medical University, Shenyang, Liaoning, 110004 People's Republic of China. | lld:pubmed |
| pubmed-article:18247312 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18247312 | pubmed:publicationType | English Abstract | lld:pubmed |
| pubmed-article:18247312 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:8487 | entrezgene:pubmed | pubmed-article:18247312 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:18247312 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:18247312 | lld:entrezgene |
