http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100973048-B1
Outgoing Links
Predicate | Object |
---|---|
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/C12Q1-6844 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
filingDate | 2007-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2010-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2010-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | KR-100973048-B1 |
titleOfInvention | Haplotype Marker Single Base Variation and Use thereof for Haplotype Analysis of Cytochrome P450 1A2 Gene |
abstract | The present invention relates to a haplotype marker single nucleotide variant (htSNP) and its use for haplotype analysis of cytochrome P450 1A2 gene, and more particularly, a method for screening htSNP for haplotype analysis of human CYP1A2 gene and the htSNP. It relates to a method for determining the genotype of the CYP1A2 gene using.n n n By using the method of the present invention, htSNP obtained on the basis of single nucleotide polymorphism (SNP) of Korean CYP1A2 gene is used in Asian ethnic groups such as Japan or China that have similar genetic characteristics to Koreans in a time and cost-effective manner. The genotype of the found CYP1A2 gene can be easily confirmed. In addition, it can be usefully used to predict individual differences in CYP1A2 enzymatic activity of Asians and abnormal symptoms caused by CYP1A2 deficiency.n n n n CYP1A2, monobasic polymorphism, haplotype, htSNP |
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: 54.