http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0042196-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-1007
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-53
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-10
filingDate 2000-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_15133cd91bd7332d17f656d556ae89d9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1f479e5608c1e49b59fb0d26b3ecf390
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f79831cce1e750200dec7166a09f797
publicationDate 2000-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-0042196-A2
titleOfInvention Human methionine synthase reductase: cloning, and methods for evaluating risk of neural tube defects, cardiovascular disease, cancer, and down's syndrome
abstract The invention features a novel gene encoding methionine synthase reductase. The invention also features a method for detecting an increased likelihood of hyperhomocysteinemia and, in turn, an increased or decreased likelihood of neural tube defects, cardiovascular disease, Down's Syndrome or cancer. The invention also features therapeutic methods for treating and/or reducing the risk of cardiovascular disease, Down's Syndrome, cancer, or neural tube defects. Also provided are the sequences of the human methionine synthase reductase gene and protein and compounds and kits for performing the methods of the invention.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107383199-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107699612-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108251541-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2013086582-A1
priorityDate 1999-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 568.