http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101158908-B1

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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/C12Q1-6883
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2010-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2012-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101158908-B1
titleOfInvention CEP68 Gene Variants Associated with Risk of Aspirin Tolerant Asthma
abstract The present invention relates to the analysis of the association between the risk of aspirin intolerant asthma and the CEP68 gene polymorphism. The present invention provides a CEP68 (Centrosomal protein 68 kDa) gene with a single base mutation for the diagnosis or prediction of aspirin intolerant asthma; And CEP68 Haplotype. The present invention also provides a method for providing information for the diagnosis or prediction of aspirin intolerant asthma using the CEP68 gene having a single base mutation. The present invention suggests that it is possible to diagnose and predict asthma associated with aspirin intolerance by analyzing the CEP68 gene polymorphism, which may be usefully used in new drug development, disease diagnosis, and treatment.
priorityDate 2010-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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