| pubmed-article:11081774 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11081774 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:11081774 | lifeskim:mentions | umls-concept:C0237401 | lld:lifeskim |
| pubmed-article:11081774 | lifeskim:mentions | umls-concept:C0063684 | lld:lifeskim |
| pubmed-article:11081774 | lifeskim:mentions | umls-concept:C0085580 | lld:lifeskim |
| pubmed-article:11081774 | lifeskim:mentions | umls-concept:C0442805 | lld:lifeskim |
| pubmed-article:11081774 | lifeskim:mentions | umls-concept:C0175630 | lld:lifeskim |
| pubmed-article:11081774 | lifeskim:mentions | umls-concept:C1517512 | lld:lifeskim |
| pubmed-article:11081774 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:11081774 | pubmed:dateCreated | 2000-11-28 | lld:pubmed |
| pubmed-article:11081774 | pubmed:abstractText | Human essential hypertension is a complex trait with poorly understood genetic determination. Insulin resistance is frequently associated with this trait. | lld:pubmed |
| pubmed-article:11081774 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11081774 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11081774 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:11081774 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11081774 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11081774 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11081774 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11081774 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11081774 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11081774 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11081774 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:11081774 | pubmed:issn | 0263-6352 | lld:pubmed |
| pubmed-article:11081774 | pubmed:author | pubmed-author:O'ConnorD TDT | lld:pubmed |
| pubmed-article:11081774 | pubmed:author | pubmed-author:HenryR RRR | lld:pubmed |
| pubmed-article:11081774 | pubmed:author | pubmed-author:ParmerR JRJ | lld:pubmed |
| pubmed-article:11081774 | pubmed:author | pubmed-author:KailasamM TMT | lld:pubmed |
| pubmed-article:11081774 | pubmed:author | pubmed-author:TyrellE AEA | lld:pubmed |
| pubmed-article:11081774 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11081774 | pubmed:volume | 18 | lld:pubmed |
| pubmed-article:11081774 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11081774 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11081774 | pubmed:pagination | 1611-20 | lld:pubmed |
| pubmed-article:11081774 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:meshHeading | pubmed-meshheading:11081774... | lld:pubmed |
| pubmed-article:11081774 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:11081774 | pubmed:articleTitle | Circulating amylin in human essential hypertension: heritability and early increase in individuals at genetic risk. | lld:pubmed |
| pubmed-article:11081774 | pubmed:affiliation | Department of Medicine and Center for Molecular Genetics, University of California and VA San Diego Healthcare System, 92161, USA. | lld:pubmed |
| pubmed-article:11081774 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11081774 | pubmed:publicationType | Clinical Trial | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11081774 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11081774 | lld:pubmed |
