http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010166844-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d75d1a4caed60a9316608ed9c231546c http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0669f10ac82c082c17a3bf9d4a941b96 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_37254d0df663eeec2aa8085ffd4f1901 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 |
filingDate | 2009-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4bc1f49e0415b2335a12a17cf3543ce7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_713f4160967cc9da57f27ff0fdcb6530 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2ddf5c130d350c5221dedac6b98983f3 |
publicationDate | 2010-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2010166844-A |
titleOfInvention | Genetic risk detection method for cerebral infarction |
abstract | A gene detection method for obtaining a material for determining a genetic risk of cerebral infarction is provided. [Solution] LLGL2 rs1671021 polymorphism, CELSR1 rs9615362, which was found by performing genome-wide association analysis (GWAS) from about 520,000 gene polymorphisms in a 6341 Japanese population. A method for detecting a genetic risk of cerebral infarction by determining a polymorphism, rs753307 polymorphism of RUVBL2. Among the nucleotide sequences of linkage disequilibrium blocks containing these polymorphisms, 3 tag SNPs and 1 non-synonymous SNP are associated with cerebral infarction, especially CELSR1 rs6007897 (A → G, Thr2268Ala) and CELSR1 rs4044210 (A → G, Ile2107Val) was an important SNP with amino acid substitution. [Selection] Figure 3 |
priorityDate | 2009-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 88.