Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_72746072af620cf031a062f4a0a4f097 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01K67-027 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N5-071 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H21-04 |
filingDate |
2011-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0eae9fdc465b41ac61cc4c3a085938f5 |
publicationDate |
2012-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
US-2012011597-A1 |
titleOfInvention |
Certain human genomic dna associated with total red-green colorblindness |
abstract |
Disclosed is human genomic DNA having the following STR marker profile: n Amel D3S1358 VWA FGA D8S1179 D21S11 D18S51 M 15-17 16-17 21-25 12-14 29-32.2 17-18 D5S818 D13S317 D7S820 CSF1PO TPOX TH01 D16S539 11-12 11-12 8-8 10-11 8-8 7-9.3 10-13 nAnd the use thereof as a reference for studying variations in the human genome that may be associated with certain genetic traits or diseases. |
priorityDate |
2007-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |