http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20110130940-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ddabaecb2b1112bb5faa3e1caff966bc |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-12 |
filingDate | 2010-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d0b9f9c2d8c119a997b9aa59cf2294f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_072f98b6d31acdc533e71ffd834589e8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a4ba24d1dd1466f0fbd26c3352beccf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a674eba258b714f3d0dc7b99e835765b |
publicationDate | 2011-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | KR-20110130940-A |
titleOfInvention | Unstructured Abnormal Diagnosis Kit |
abstract | The present invention relates to a mutant SOHLH1 gene which is a cause of nonstructural aberrant dementia and a diagnostic kit capable of diagnosing a nonstructural aberrant atresia by detecting a mutation of the gene. The non-structural abnormality diagnosis kit of the present invention is a primer (SEQ ID NO: 1) capable of detecting three genetic variations (c.91TC, c.346-1GA and c.529CA) in the nucleotide sequence of the SOHLH1 gene. To 6). By using the non-structural abnormality-determination diagnostic kit of the present invention, it is possible to more easily identify the non-structural abnormality-determination, it will be widely used in more effective infertility treatment. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113512581-A |
priorityDate | 2010-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 23.