http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112037848-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3bb0ff26afb9eb59ecacbc9911eaca1d |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B15-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B30-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B20-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G16B50-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B30-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B50-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B15-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G16B20-20 |
| filingDate | 2020-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_68bf2db5a3a50bde8f6eae0cd44a65a6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9cac49a8e9ba44f2feab3794996abed8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14047fe5f5f342bb61819eb7c9794743 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_719f7fcc9825f363ed86fc37a8574ed6 |
| publicationDate | 2020-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-112037848-A |
| titleOfInvention | Non-small cell lung cancer gene variation and medication interpretation system, interpretation method and device |
| abstract | The specification provides a non-small cell lung cancer genetic variation and medication reading system, a non-small cell lung cancer genetic variation and medication reading method and a non-small cell lung cancer medication reading device, wherein the system comprises a non-small cell lung cancer database version, the database version comprises a plurality of databases which are mutually associated through the same key field or the same key field combination, and the databases are respectively used for storing relevant information of non-small cell lung cancer; when the analysis is carried out, carrying out biological information analysis on the sequencing off-line data of the detected sample to obtain the genetic variation annotation information of the detected sample; the sequencing off-line data comprises sample information of a detected sample; and performing correlation reading on the sample information and the genetic variation annotation information of the detected sample and a database in the database version block to obtain the corresponding interpretation information of the detected sample. When the non-small cell lung cancer gene variation and medication interpretation system is used for medication interpretation, a comprehensive medication guidance suggestion with clear evidence grade can be quickly and accurately found and provided, and an important reference is provided for medical decision. |
| priorityDate | 2020-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 152.