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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883
filingDate 2021-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-112708673-B
titleOfInvention Application of PRDM9 transposon fusion as congenital megacolon disease marker
abstract The invention relates to the field of biomedicine, in particular to application of PRDM9 transposon fusion as a congenital megacolon disease marker. The fusion site of the PRDM9 transposon fusion is selected from PRDM9-type I located at chr5: 23299411; PRDM9-type II-1 at chr5: 23262356; and PRDM9-type II-2 at chr5: 23245181. Compared with the traditional diagnosis method (barium enema and the like), the method has the advantages of simple and quick operation, no intervention, high flux, low cost and the like.
priorityDate 2021-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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