http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0178314-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2770-00022
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-005
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-10
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filingDate 1985-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_137e0a9f399ee62b5b4c27e557717de0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_823288c0db82057357cbc10e94e1f1a7
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publicationDate 1986-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0178314-A1
titleOfInvention An improved method of cloning double-stranded rna, and its use in the production of viral gene clones
abstract A method of directly inserting double-stranded RNA into a cloning vector formed of double-stranded DNA, comprising a) isolating dsRNA from a source of interest; b) if necessary, uncapping the dsRNA; and c) direct ligation of dsRNA to dsDNA of the appropriate cloning vector. This process allows direct cloning of dsRNA, thereby eliminating the traditional step of first making a copy by complementary DNA of the RNA molecule. Thanks to this process, it is possible to construct probes for the detection of viral diseases in plants and animals. This process can also be used to produce new plant strains resistant to a particular virus, or to confer animal immunity to a specific virus.
priorityDate 1984-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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