http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2013202634-B2

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_803023bbcbd1fcfd4f7ad657d38cae1a
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-48
filingDate 2013-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b3d1df8c6b4b50a9628433283de9b34
publicationDate 2016-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2013202634-B2
titleOfInvention Method of identifying disease risk factors
abstract Provided herein is a method for identifying a genetic variant that is associated with development of a condition of interest (e.g,, Alzheimer's disease), and genetic variants so identified. Methods of treatment with an active agent (e.g., with a particular active agent and/or at an earlier age) is also provided, upon detecting a genetic variant described herein. In some embodiments, the genetic variant is a deletion/insertion polymorphism (DIP) of the TOMM40 GENE. Kits for determining if a subject is at increased risk of developing late onset Alzheimer's disease is also provided. Kits for determining if a subject is responsive to treatment for a condition of interest with an active agent are further provided.
priorityDate 2008-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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