http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5614372-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K16-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-574
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K16-40
filingDate 1995-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d29ca880e97e861cddc010dad35bf8b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55db5d8524b1d98ecae9cc247b2c66e3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ecaa5e666925f3e003e2846f878bfba8
publicationDate 1997-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5614372-A
titleOfInvention Early detection of prostate cancer (CAP) by employing prostate specific antigen (PSA) and human glandular kallikrein (hGK-1)
abstract The invention relates to a bioaffinity assay of prostate-specific antigen (PSA) comprising the measurement of either the concentration of total PSA (PSA-T), the concentration of free form of PSA (PSA-F) or the concentration of PSA complexed to alpha-1-antichymotrypsin (PSA-ACT), PSA-T being the sum of PSA-F and PSA-ACT. According to the invention, additionally the concentration of human glandular kallikrein (hGK-1) is measured. The concentrations of PSA-T and hGK-1 can be measured in one single assay or in separate assays. The sum of the concentrations of PSA-T and hGK-1 is used to determine the ratio a) PSA-F/(PSA-T+hGK-1) and/or b) PSA-ACT/(PSA-T+hGK-1). Both of these ratios are shown to have clinical utility for the discrimination of prostate cancer and benign prostatic hyperplasia.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2009036544-A1
priorityDate 1995-02-24-04:00^^<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: 59.