http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2021310073-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_78587acbfc8d4c9e9ac3baa7021087d7 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
| 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/C12Q1-6827 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 |
| filingDate | 2019-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2da32ea8eac9f3f29451ded2708e1c14 |
| publicationDate | 2021-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-2021310073-A1 |
| titleOfInvention | A genetic predisposition to liver disease |
| abstract | Embodiments of the disclosure concern a genetic signature for individuals suspected of having liver disease, including end stage liver disease. In particular embodiments, the genetic signature comprises two different genetic markers, including a polymorphism and differential probe hybridization. In specific embodiments, the polymorphism is the rs4567 SNP in the 3′ UTR of the MAN1B1 and the copy number variation is in chromosome 22. |
| priorityDate | 2018-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 43.