http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2601308-A1

Outgoing Links

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2011-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8f5be46ea5508c8ef0f15b0e56dc723
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_104a080b96be94353308d6aec7d9397f
publicationDate 2013-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2601308-A1
titleOfInvention Aspp2 splicing variant
abstract The invention relates to a method for the in vitro determination of the presence of or a predisposition of a patient to the development of cancer. The presence of a marker is determined in a biological sample of the patient, said marker being selected from a) the amino acid sequence SEQ ID Nr. 2 from the sequence protocol that is provided, or b) a nucleic acid that encodes the amino acid sequence with the SEQ ID Nr. 2. The invention further relates to the amino acid and the encoding nucleic acid and to the use thereof in diagnostics and for molecular therapeutic approaches.
priorityDate 2010-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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