About: Klaus Lindpaintner

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Attributes	Values
rdf:type	Item
description	rakouský lékař a výzkumný pracovník, zabývá se genetikou a kardiovaskulárními chorobami, působí v Americe (cs)
rdfs:label	Klaus Lindpaintner (cs) Klaus Lindpaintner (en) Klaus Lindpaintner (sk)
skos:prefLabel	Klaus Lindpaintner (cs) Klaus Lindpaintner (en) Klaus Lindpaintner (sk)
name	Klaus Lindpaintner (cs) Klaus Lindpaintner (en) Klaus Lindpaintner (sk)
given name	wds:Q112434959-1F12F4C1-232C-4883-88C5-1F3696B7BAC5
given name	Klaus
instance of	wds:Q112434959-FDAA29B7-B3E8-4A85-AFEB-D5C79A6DC0BF
NL CR AUT ID	wds:Q112434959-917675B1-49D1-4B5B-A99A-D2F56667AB01
instance of	Homo sapiens
NL CR AUT ID	mub2010613781
skos:altLabel	K. Lindpaintner (cs) Klaus Lindpainter (cs)
occupation	wds:Q112434959-4DD6E2A8-4170-44C8-A823-BE1A8F1EFAEB
NUKAT ID	wds:Q112434959-2A75883C-03FD-48BF-9F42-F8CACA491B68
languages spoken, written or signed	wds:Q112434959-60E85E61-7F46-4D30-BC1C-360922367181
sex or gender	wds:Q112434959-6D30FD73-85FE-4B4F-8F39-9B0547A5E195
ISNI	wds:Q112434959-112A1844-9ED6-4AD2-975E-A758E742474D
VIAF ID	wds:Q112434959-593D911B-9837-4A0D-8020-7DB7E813C9B8
IdRef ID	wds:Q112434959-f44e7a5f-7970-4ac6-bb54-c6c3a43b52c3
date of birth	wds:Q112434959-985A281E-4527-400E-B59D-4794A4CBD101
family name	wds:Q112434959-E84AE165-7056-493C-AA2B-EC31C0FA7CA6
National Library of Israel J9U ID	wds:Q112434959-0FB94ED7-B4DE-41AA-8F83-95C0484C3355
VIAF ID	http://viaf.org/viaf/23820317
IdRef ID	http://www.idref.fr/198363427/id
occupation	physician
NUKAT ID	n2012250860
languages spoken, written or signed	English
sex or gender	male
ISNI	0000000067643677
VIAF ID	23820317
IdRef ID	198363427
date of birth	1955-01-01 00:00:00Z (xsd:dateTime)
family name	Lindpaintner
National Library of Israel J9U ID	987007313049505171
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q112434959
is author of	Polymorphism in the P-selectin and interleukin-4 genes as determinants of stroke: a population-based, prospective genetic analysis. A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients Homocysteine, 5,10-methylenetetrahydrofolate reductase 677C>T polymorphism, nutrient intake, and incident cardiovascular disease in 24,968 initially healthy women Polymorphism in the beta2-adrenergic receptor and lipoprotein lipase genes as risk determinants for idiopathic venous thromboembolism: a multilocus, population-based, prospective genetic analysis Alanine for proline substitution in the peroxisome proliferator-activated receptor gamma-2 (PPARG2) gene and the risk of incident myocardial infarction A prospective study of TaqIB polymorphism in the gene coding for cholesteryl ester transfer protein and risk of myocardial infarction in middle-aged men. Threonine for alanine substitution in the eotaxin (CCL11) gene and the risk of incident myocardial infarction C-reactive protein gene variation and type 2 diabetes mellitus: a case-control study. Intercellular adhesion molecule 1 (ICAM1) Lys56Met and Gly241Arg gene variants, plasma-soluble ICAM1 concentrations, and risk of incident cardiovascular events in 23,014 initially healthy white women. Erratum to “A prospective study of TaqIB polymorphism in the gene coding for cholesteryl ester transfer protein and risk of myocardial infraction in middle-aged men”
is author of	wds:Q44928864-44055FA2-5A47-4D92-9258-F0B27155D13D wds:Q46930237-C6879FC8-9115-42D7-BFAF-DCAF2A6CCE87 wds:Q34117782-44FD2C2A-7CEB-4F8E-90BE-784C710E261B wds:Q83228734-8E51AC24-D688-4F85-9023-F8895936B2C8 wds:Q34509923-CF9BD0F7-0B98-4F50-B097-03E08A95B4DC wds:Q37365047-EA4A33B6-4BF8-44F8-9AE2-9136C8A0D933 wds:Q47313978-1AC68C3E-04D8-48E0-AB03-2C1356B21E83 wds:Q46948906-A8E76A37-B62F-4321-ABE8-ECEFA523759A wds:Q57616852-1385AB2C-1D88-4EA3-A51D-8D84D1AC0761 wds:Q79855746-F7A3A4B5-CE22-4F40-887C-CE436AAE49C3

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