http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1538220-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_43b7eaab4a227ee4cebb5c873862ced2
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/C12Q1-68
filingDate 2003-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_104ae9734b1ebd9266ee89f6c76e8017
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_59809d2e745de920287619fa1fa7d28d
publicationDate 2005-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1538220-A2
titleOfInvention Allelic variants in the factor vii gene
abstract The presence of at least one of said allelic variantsnaffects the stability and/or functionality of the nucleicnacid molecule and/or of the product coded by said nucleicnacid molecule. n The procedure for analyzing a nucleic acid moleculencomprises obtaining said molecule from a biological samplenand determining at least one allelic variant from Table 1,nsaid allelic variant affecting the stability and/ornfunctionality of the nucleic acid molecule and/or of thenproduct coded thereby. n The isolated product coded by a nucleic acid moleculenwhich includes at least one allelic variant can be used asna medicament.
priorityDate 2002-07-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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