http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022010917-A9

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827
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/C12Q1-6827
filingDate 2021-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8a52709f91191e02a94cb32fd001193c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_78b11951a56385c7a956ef9fa3ac0369
publicationDate 2022-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2022010917-A9
titleOfInvention Methods, compositions, and systems for detecting pnpla3 allelic variants
abstract Disclosed herein are methods and kits for detection of a single nucleotide polymorphism (SNP) rs738409 of a Patatin-like phospholipase domain containing 3 (PNPLA3) gene in a subject. Such methods are useful in the diagnosis of a subject with NASH and the selection of a particular treatment for the subject. In some embodiments, the provided methods allow for a highly selective detection of SNP rs738409, in the presence or absence of an insertion variant upstream of exon 3.
priorityDate 2020-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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