http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2003219886-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_251e1845f2afb83192254fcce85de629 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
filingDate | 2002-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44a732d1bdd662427c208372f8b18e07 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ff89020dac014c14be93057cb2523b4 |
publicationDate | 2003-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2003219886-A |
titleOfInvention | Nucleic acid containing single nucleotide polymorphism in protein 1 gene and method for diagnosing protein 1 related disease using the same |
abstract | (57) [Problem] To provide a method of diagnosing a protein 1-related disease by using a molecular genetic technique different from a conventional immunological technique in order to enable a multifaceted diagnosis of a protein 1-related disease. . The present invention provides a method for diagnosing a protein 1-related disease by detecting a mutation in the nucleotide sequence of human chromosome 11 q12.3 to q21 contained in a sample, wherein the mutation determines the protein transcription start position. As a reference, mutation at the -908 base, mutation at the 118 base, mutation at the 1225 base, 1 The present invention relates to the diagnostic method, further comprising one or more mutations selected from the group consisting of a mutation at the 226th base and a mutation at the 4777th base. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2005093059-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2005093059-A1 |
priorityDate | 2002-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 35.