| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ebc60274eb6f304fcecb89be02d451a2 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate |
1996-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f7f96b69f02aa06f96125b5eb532bb9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f7dc5e0598d6f645fdcb71ae87ceb921
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_db22ceaf9ab88e006099754d02bf6139 |
| publicationDate |
1998-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
JP-H1099099-A |
| titleOfInvention |
Method for diagnosing human LDL receptor gene abnormality, and probe and oligonucleotide primer used therein |
| abstract |
(57) [Problem] To provide means for diagnosing an unknown abnormality of a human LDL receptor gene which has not been reported so far. SOLUTION: A method for diagnosing a human LDL receptor gene abnormality, which comprises examining whether the nucleotide sequence of codon 109 of exon 4 of the human LDL receptor gene is TCA or whether C is inserted into TCCA to TCCA. Offered. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100443503-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012080835-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110592185-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004067740-A1 |
| priorityDate |
1996-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |