http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CZ-2011578-A3

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-50
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-12
filingDate 2011-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6347f07ad5677ec6191285bd98b18e0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52e51bc1740faabff23fd9bd8976b1a3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_461a8c150324b42cd9bc74295934aebc
publicationDate 2012-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-2011578-A3
titleOfInvention Method of identifying persons with increased genetic risk of myocardial infarction
abstract The solution describes a method of identifying persons with increased genetic risk of acute myocardial infarction and a low risk of subsequent death due to cardiovascular complications at a time horizon of up to 6 months from the onset of cardiac events, in which the biological sample taken from the patient's body determines the intensity gene expression and genetic loci of OLIG2, VNN3, MS4A3, CEBPE, FOS, LIPA, LOC645649, (M97723), EPAS1, CLINT1, MYCT1, VPS29 and LOC 130951. The logarithmic expression level of base 2 is then compared to the expression intensity reference value, wherein the deviation from the reference value being at least the minimum deviation for all of said genes and genetic loci is an increased risk.
priorityDate 2011-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID84128
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID395765
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP01295
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID2540882

Total number of triples: 319.