http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2063381-C1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_601aea756a699025b0af6f88c48fe4bf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24beed2ee11f430ab3acb1e6a1f85668
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-68
filingDate 1988-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1996-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2ee5369bbfba3544a06e67a74a5b429a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cfabb877168297f9e59fcd1ccfc8e6e7
publicationDate 1996-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2063381-C1
titleOfInvention Process for determining exacerbation of diffusion liver disease
abstract FIELD: medicine. SUBSTANCE: process comprises sampling 1 ml of blood serum, pouring 0.5 ml of 10% trichloroacetic acid thereto, centrifuging the whole at 3000 rpm for 30 minutes, separating supernatant liquid, diluting it with distilled water at 1:9 ratio and subjecting the mixture to spectrophotometry at wavelength of 280 nm, and at value of 0.355 or more, determining exacerbation of diffusion liver disease. EFFECT: more accurate early diagnostics of active phase.
priorityDate 1988-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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