http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2015167083-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_82cbc291d77c061ac9a216f86ec010a3 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-154 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2012-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34089839486c0409c4a2b316b3ff7b3d |
| publicationDate | 2015-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-2015167083-A1 |
| titleOfInvention | Method for assessing risk of imprinting disorder |
| abstract | The present invention provides a method for assessing the risk that the progeny of a subject would develop an imprinting disorder, which comprises extracting genomic DNA from sperm collected from the subject, and measuring the methylation level of a CpG sequence comprised in the differentially methylation region of one or more maternally imprinted genes selected from the group consisting of DIRAS3, NAP1L5, FAM50B, GRB10, INPP5Fv2, RB1, ZNF597, ZNF331, PSIMCT-1, NNAT, L3MBTL, NESPAS, and GNAS1A, in the genomic DNA. According to the present invention, it becomes possible to safely and accurately assess the risk that the progeny of a subject would develop an imprinting disorder, using sperm collected from the subject. |
| priorityDate | 2012-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 63.