pubmed-article:20124734 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20124734 | lifeskim:mentions | umls-concept:C0020443 | lld:lifeskim |
pubmed-article:20124734 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
pubmed-article:20124734 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:20124734 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
pubmed-article:20124734 | lifeskim:mentions | umls-concept:C1863512 | lld:lifeskim |
pubmed-article:20124734 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
pubmed-article:20124734 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
pubmed-article:20124734 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:20124734 | pubmed:dateCreated | 2010-2-26 | lld:pubmed |
pubmed-article:20124734 | pubmed:abstractText | The autosomal recessive hypercholesterolemia (ARH) gene is located on chromosome 1p35 and encodes a 308-amino acid protein containing a phosphotyrosine-binding domain. Several researchers have identified mutations of ARH that cause autosomal recessive hypercholesterolemia; however, it remains unknown whether this gene is involved in common hypercholesterolemia. | lld:pubmed |
pubmed-article:20124734 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20124734 | pubmed:language | eng | lld:pubmed |
pubmed-article:20124734 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20124734 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:20124734 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20124734 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20124734 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20124734 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20124734 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20124734 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20124734 | pubmed:month | Feb | lld:pubmed |
pubmed-article:20124734 | pubmed:issn | 1880-3873 | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:TomoikeHitono... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:SaitoYoshihik... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:MiyamotoYoshi... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:MakinoHisashi... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:KokuboYoshihi... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:OkayamaAkiraA | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:HaradaKojiK | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:OkamuraTomono... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:YoshimasaYasu... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:MorisakiTakay... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:MorisakiHirok... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:Harada-ShibaM... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:YamanakaItaru... | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:OhtaNaotakaN | lld:pubmed |
pubmed-article:20124734 | pubmed:author | pubmed-author:TomonoriOkamu... | lld:pubmed |
pubmed-article:20124734 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20124734 | pubmed:day | 26 | lld:pubmed |
pubmed-article:20124734 | pubmed:volume | 17 | lld:pubmed |
pubmed-article:20124734 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20124734 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20124734 | pubmed:pagination | 131-40 | lld:pubmed |
pubmed-article:20124734 | pubmed:dateRevised | 2010-6-22 | lld:pubmed |
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pubmed-article:20124734 | pubmed:meshHeading | pubmed-meshheading:20124734... | lld:pubmed |
pubmed-article:20124734 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20124734 | pubmed:articleTitle | A novel Thr56Met mutation of the autosomal recessive hypercholesterolemia gene associated with hypercholesterolemia. | lld:pubmed |
pubmed-article:20124734 | pubmed:affiliation | Department of Atherosclerosis and Diabetes, National Cardiovascular Center, Osaka, Japan. | lld:pubmed |
pubmed-article:20124734 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20124734 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
entrez-gene:26119 | entrezgene:pubmed | pubmed-article:20124734 | lld:entrezgene |
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