http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2022101948-A1

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filingDate 2021-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_990e7473d6379ecb53439bbf7187596f
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publicationDate 2022-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2022101948-A1
titleOfInvention Methods of identifying genetic variants
abstract The present invention relates to identification of an abnormal splice site. Provided are methods of identifying an abnormal splice site. Methods of classifying the risk of abnormal splicing of a splice site are also provided. Databases for use in the methods provided herein are also disclosed.
priorityDate 2018-11-15-04:00^^<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/gene/GID1444131
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCC3NEV8
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCB1I8S4
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID100009074
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCB5XZL2
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID477032
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID672
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID12290
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Total number of triples: 634.