| pubmed-article:20634323 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20634323 | lifeskim:mentions | umls-concept:C0085756 | lld:lifeskim |
| pubmed-article:20634323 | lifeskim:mentions | umls-concept:C0229671 | lld:lifeskim |
| pubmed-article:20634323 | lifeskim:mentions | umls-concept:C0017661 | lld:lifeskim |
| pubmed-article:20634323 | lifeskim:mentions | umls-concept:C0441889 | lld:lifeskim |
| pubmed-article:20634323 | lifeskim:mentions | umls-concept:C0020840 | lld:lifeskim |
| pubmed-article:20634323 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:20634323 | pubmed:dateCreated | 2010-11-8 | lld:pubmed |
| pubmed-article:20634323 | pubmed:abstractText | Serum levels of galactose-deficient IgA1 (Gd-IgA1) are elevated and heritable in Caucasian and Asian patients with IgA nephropathy (IgAN), but have not been characterized in African Americans (AA). Our objective was to determine whether serum Gd-IgA1 levels are increased in AA patients with IgAN and whether this is a heritable trait in this group. | lld:pubmed |
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| pubmed-article:20634323 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20634323 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20634323 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20634323 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20634323 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20634323 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:20634323 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20634323 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20634323 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:20634323 | pubmed:issn | 1555-905X | lld:pubmed |
| pubmed-article:20634323 | pubmed:author | pubmed-author:MoldoveanuZin... | lld:pubmed |
| pubmed-article:20634323 | pubmed:author | pubmed-author:NovakJanJ | lld:pubmed |
| pubmed-article:20634323 | pubmed:author | pubmed-author:JulianBruce... | lld:pubmed |
| pubmed-article:20634323 | pubmed:author | pubmed-author:GharaviAli... | lld:pubmed |
| pubmed-article:20634323 | pubmed:author | pubmed-author:WyattRobert... | lld:pubmed |
| pubmed-article:20634323 | pubmed:author | pubmed-author:McGlothanKim... | lld:pubmed |
| pubmed-article:20634323 | pubmed:author | pubmed-author:HastingsM... | lld:pubmed |
| pubmed-article:20634323 | pubmed:author | pubmed-author:SandersJohn... | lld:pubmed |
| pubmed-article:20634323 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20634323 | pubmed:volume | 5 | lld:pubmed |
| pubmed-article:20634323 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20634323 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20634323 | pubmed:pagination | 2069-74 | lld:pubmed |
| pubmed-article:20634323 | pubmed:dateRevised | 2011-11-1 | lld:pubmed |
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| pubmed-article:20634323 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20634323 | pubmed:articleTitle | Galactose-deficient IgA1 in African Americans with IgA nephropathy: serum levels and heritability. | lld:pubmed |
| pubmed-article:20634323 | pubmed:affiliation | Children's Foundation Research Center at Le Bonheur Children's Medical Center, Memphis, TN 38103-2893, USA. | lld:pubmed |
| pubmed-article:20634323 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20634323 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:20634323 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:20634323 | lld:pubmed |
