http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20080023622-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_745a75b0350f49480798ef5ab913bc0a |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-172 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2007-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd593ef4bf48ae7b7c5685add0a23220 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d303fd27ed9ea783fd1fa84eed1185d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11d1a73c7f3c91bcb1fd5e155a511923 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39b13ff5ea22c51fee186f9d2e1774c7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_64a20842007f784e770264f778da0bdc |
| publicationDate | 2008-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-20080023622-A |
| titleOfInvention | Haplotype marker single base mutation and genotyping chip using the same for genotyping of cytochrome P450 2di6 gene |
| abstract | The present invention relates to a haplotype marker single nucleotide variant (htSNP) for genotyping of cytochrome P450 2D6 gene and a gene chip using the same, and more particularly, to a method for screening htSNP for haplotype analysis of human CYP2D6 gene. The present invention relates to a method for determining the genotype of the CYP2D6 gene using htSNP and a genotyping chip for the same.n n n By using the method of the present invention, htSNP obtained on the basis of single nucleotide polymorphism (SNP) of Korean CYP2D6 gene is used in Asian species such as Japan or China, which have similar genetic characteristics to Koreans in a time and cost-effective manner. Variants of the found CYP2D6 gene can be easily identified. In addition, it can be usefully used to predict individual differences in CYP2D6 enzymatic activity of Asians and abnormal symptoms that may be caused by CYP2D6 deficiency. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2021029473-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20210020253-A |
| priorityDate | 2006-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 271.