http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20080111192-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/C12Q2600-172 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6844 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2007-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36abbf58ad094812da9383e7a735c5bc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c594b0a6e07fac51608986f29582f7ee http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd593ef4bf48ae7b7c5685add0a23220 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07b42b0e8a5c24cf827049ec5406abbf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e73f8a7e935ce4273b855f266a5a1c41 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_64a20842007f784e770264f778da0bdc |
| publicationDate | 2008-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-20080111192-A |
| titleOfInvention | Haplotype Marker Single Base Variation and Uses thereof for the Functional Variation Analysis of Pregnan X Receptor Genes |
| abstract | The present invention relates to haplotype marker single nucleotide variants (htSNPs) and uses thereof for the functional variant analysis of Pregnane X receptor (PXR) genes, and more particularly to folds of functional variations of human PXR genes. The present invention relates to a method for screening htSNP for body type analysis and a method for determining functional variants of the PXR gene using the htSNP.n n n By using the method of the present invention, the HTSNP obtained based on single nucleotide polymorphism (SNP) of Korean PXR gene was used to detect PXR genes found in Asians with similar genetic characteristics to Koreans. Functional variants can be easily identified. In addition, it can be usefully used to predict individual differences in PXR activity of Asians or abnormal symptoms that may be caused by PXR deficiency. |
| priorityDate | 2007-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 276.