http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106947824-B

Outgoing Links

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11
filingDate 2017-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2019-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106947824-B
titleOfInvention The variant sites and its detection method and purposes of obstruction sleep apnea-hypopnea syndrome tumor susceptibility gene ADIPOQ
abstract The present invention relates to molecular biology and medical domain, the invention discloses the variant sites of obstruction sleep apnea-hypopnea syndrome tumor susceptibility gene ADIPOQ and its detection method and the variant sites obstruction sleep apnea-hypopnea syndrome neurological susceptibility context of detection purposes, furthermore a kind of method for predicting obstruction sleep apnea-hypopnea syndrome risk by detecting the variant sites genotype is also disclosed, genomic DNA including extracting sample, specific amplification, detection, variant sites genotyping and etc., when genotypic variation occurs for the site, the risk of obstruction sleep apnea-hypopnea syndrome increases.The invention also discloses a kind of kits for detecting obstruction sleep apnea-hypopnea syndrome neurological susceptibility.
priorityDate 2017-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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