http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-102017018274-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0ac2c2182e722253ed39dd9c2ff9b586
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-70
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6888
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6853
filingDate 2017-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de1330ff01cd19a11bf30b485ea8a1d1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b1a219d5397f7f8ec9171113d18da15d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8a02e1e544b8b16d8c0c729c9641e43d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_33f4bc2df16293fead2f33284d68715c
publicationDate 2019-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-102017018274-A2
titleOfInvention NUCLEIC ACID SEQUENCES AND THEIR USE FOR DETECTION AND TYPING OF HUMAN PAPILOMAVIRUS
abstract The present invention consists of synthetic nucleic acid sequences, also called oligonucleotides, primers or DNA primers, and their use for the detection and typing of human papillomavirus (hpv) genotypes in samples containing human cells. The oligonucleotides that make up the present invention bind to specific regions in the gene encoding the e1 replication protein in the hpvs genome, allowing the generation of a measurable marker that determines the presence of the virus and enables typing by the reaction technique. DNA polymerase chain (pcr) and related techniques such as real-time pcr and insulated isothermal pcr, or by hybridization with labeled probes (southern blot or northern blot).
priorityDate 2017-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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