Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_eb9c6b40161bafe7bd55f0b4defcea04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bef12704672c84e75912a3db9884efea http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a8d58c92ff6abc3740cf5c0d34e52b86 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2537-113 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2539-105 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2565-131 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2537-143 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
filingDate |
2008-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate |
2014-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_95838fc9620413e8a5f705f28e533a2c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a8e6fd1993861b048169989641be06f |
publicationDate |
2014-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
US-8906620-B2 |
titleOfInvention |
Exon grouping analysis |
abstract |
This invention pertains to the identification of specific disease-causing DNA sequences in a subject. The methods of the present invention can be used to identify genetic alterations, to determine the molecular basis for genetic diseases, and to provide carrier and prenatal diagnosis for genetic counseling. |
priorityDate |
2007-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |