Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1d7e470e09803bd6bf24b2fd176109dd http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_43a72884e25aaecffebe0942132d704f |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-172 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-12 |
filingDate |
1998-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5adccf3b8600d6b0718a1d7b4d4e99dd http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82db8f9cb6b2c9170e9764017a1162b4 |
publicationDate |
1998-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
CA-2292795-A1 |
titleOfInvention |
Indirect genotypic method for diagnosing type 2 familial hemiplegic migraine |
abstract |
The present invention relates to a method of indirect genotypic diagnosis familial hemiplegic migraine type 2 in an individual, characterized in that: it highlights in the DNA of said individual the presence of a marker located on chromosome 1q21-q23 in the locus bounded by markers D1S2343 and D1S2844, said marker being linked to the occurrence of familial hemiplegic migraine within the family. |
priorityDate |
1997-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |