Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0a910d33c239980f3a705e312c5bad6a |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P19-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P19-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-88 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P19-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P19-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-7088 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-88 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K48-00 |
filingDate |
2001-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9c163d4d1f4d8687ee8bbc3aa92687d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dda863bf5524350bf29f9064c1e3dedb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89f43e6245c2cbb4bde472b8f7ce0378 |
publicationDate |
2001-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
JP-2001286288-A |
titleOfInvention |
Diagnostic method |
abstract |
(57) [Summary] (Modified) [Problem] Human plastaglandin E2 receptor 1 (EP1- R) To provide polymorphisms in the gene and the corresponding novel allelic polypeptides encoded thereby. SOLUTION: The sequence of one or more positions of a specific site in the EP1-R gene of human nucleic acid, or EP1- Determination of the amino acid sequence at position 126 or 154 of the R protein; and diagnosis of EP1-R gene polymorphism in humans, including determination of the human condition with reference to the polymorphism in the EP1-R gene or protein. Is done. |
priorityDate |
2000-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |