http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0721013-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3c7d1e0bf0efe57c98ba543afd5bf966
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_884170daee0baff8400371fa096c4d27
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K38-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-31
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-31
filingDate 1995-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_020ab1894d54765b5445d10c35a32a66
publicationDate 1996-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0721013-A1
titleOfInvention New staphylokinase derivatives
abstract The invention relates to staphylokinase derivatives showing a reduced immunogenicity as compared to wild-type staphylokinase. To achieve this the invention provides staphylokinase derivatives having essentially the amino acid sequence of wild-type staphylokinase but wherein at least one immunodominant epitope is eliminated without destroying the biological activity of the derivatives.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1724282-A3
priorityDate 1995-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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