http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006180876-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dfd617dc43a4c986d2dd81e4cb39d9dd http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c2d6cc21bc7bce139ac89fd102222f74 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53 |
| filingDate | 2005-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b84456081b346d4dccb94692ebb44551 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_beb96fb267e74e0864f5bb0ca663829d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20d4b8bafae90d78b3bc584458e034d9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_02e9c984d399d8f72197e9000f7a6f28 |
| publicationDate | 2006-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2006180876-A |
| titleOfInvention | Detection method of gene mutation related to thrombotic disease by P2Y12 receptor gene analysis |
| abstract | The present invention provides a means for enabling early diagnosis of thrombotic diseases and determination of morbidity risk. And means for detecting four kinds of one base mutation present upstream of exon 2 in the genome sequence of A P2Y 12 receptor gene, can cause a thrombotic disease (peripheral artery disease, coronary artery disease and stroke, etc.) A method for detecting a genetic mutation having sex, a method for examining the risk of thrombotic disease using the detection method, a gene having the single nucleotide mutation, a polynucleotide and a reagent kit used in the method. |
| priorityDate | 2004-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 35.