| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_58c8cf5e272691db3c376434b0aa7f99
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e0daec85fdd4a4c04e22225e70a5cd9 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K2317-565
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K2317-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2800-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2800-60 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K16-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K16-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K16-2809
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6893
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6848 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01J49-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-725
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K16-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-577 |
| filingDate |
2019-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13b2409aafc795fa395f8b8e35c02518
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1cfadac11ccc3188785373def76c248b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1a85ca7c82b29bee251981e64cb847c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cce8bec065b6ff2a1d79753d9cf2b1f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bcd00684c3c4446d90b7dc5b7f40856a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fb9c018b36678267d9b0be42d17d1f1c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9e5a855846d3b3544a0cb194758db6d |
| publicationDate |
2021-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
EP-3861018-A1 |
| titleOfInvention |
Newborn screening for primary immunodeficiencies, cystinosis, and wilson disease |
| abstract |
Newborn screening for primary immunodeficiencies, cystinosis, and Wilson disease is described. The newborn screening can detect these disorders from dried blood spots already routinely collected at the time of birth. Early detection of these disorders will greatly improve patient outcome as each of them can be fatal once symptoms emerge. |
| priorityDate |
2018-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |