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filingDate 2012-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2017-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103747805-B
titleOfInvention For treating, delaying and/or preventing human genetic disease's such as type of steirert-Batten-Gibb syndrome 1（DM1）Compound
abstract The present invention is provided to treat, delay and/or prevent the noval chemical compound of human genetic disease, human genetic disease type of myotonia dystrophy 1 as caused by the CUG Repeated expansions in the transcript as DM1/DMPK, SCA8 or JPH3 gene（DM1）, the type of spinocebellar ataxia 8 and/or the type of Huntington's disease sample 2.
priorityDate 2011-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCO35736
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID44124149
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ673L6
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22140692
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9Z518
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419488681
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9HSS7
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454521068
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ90YI0
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP17721
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID7273
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP08505
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ4KTA7
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9Z7T0
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA4FZL2
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA0A803JUX3
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP23722
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Total number of triples: 442.