http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004191785-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6886
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-68
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filingDate 2000-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b97f49eaf430197e6b0197cf28946542
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fcecf1e49818aa4650c5efc49a61549a
publicationDate 2004-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004191785-A1
titleOfInvention Methods for diagnosing individuals with an increased risk to develop a deficiency based on mdr1 gene polymorphism
abstract The present invention relates to in vitro methods of diagnosing an increased risk to develop a renal, liver or colon deficiency, a deficiency in lymphoid cells or a deficiency at the blood brain barrier. Furthermore, the present invention also relates to the use of a MDR-1 gene single nucleotide polymorphism for the preparation of a diagnostic composition for diagnosing a renal, liver or colon deficiency, a deficiency in lymphoid cells or a deficiency at the blood brain barrier. Preferably, the renal, liver or colon deficiencies, the deficiency in lymphoid cells or the deficiencies at the blood brain barrier are caused by cancer.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8835115-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010247481-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006133841-A1
priorityDate 2000-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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