http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-I712693-B

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filingDate 2018-05-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c845f0aa4260b049577e1f7f8f90ab4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f84855f2d6c61fef6508a2b93835c5e6
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publicationDate 2020-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-I712693-B
titleOfInvention Method for detecting snp sites on smn gene
abstract A method for detecting a SNP site of SMN genes is disclosed, and includes the steps of: (S10) performing a polymerase chain reaction (PCR) for amplifying a nucleic acid fragment including the SNP site; (S20) performing a dephosphorylation reaction on the nucleic acid fragment; (S30)performing an extension reaction on the nucleic acid fragment, wherein an extension primer is provided to identify the location of the SNP site and a single nucleotide complementary to the base of the SNP site is extended from the 3’ end of the nextension primer, so that at least one extended extension primer is obtained; (S40) performing a purification reaction; and (S50) detecting the molecular weight of the at least one extended extension primer for determining a type of a base of the SNP site based upon the molecular weight, thereby determining whether SMN1 gene homozygous deletion occurs based upon the type of the base of the SNP site.
priorityDate 2018-05-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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