| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bd0226bc5956444f686893e2aea57281
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_352521b1e3fad056bf41613bbaed0bd5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c4c0500415e2ccf0e691a18b6d6b9ca3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f34119b232d292c72e632b62008eca90 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2320-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N2310-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-113
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6809
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-14 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate |
2008-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a0f139c6fdf39cdce6cc0cd732791ee
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54534b982c62825bab9df7edd6d6e7dd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00c02f28babce62a9d926bf1004a007a |
| publicationDate |
2008-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
WO-2008147930-A2 |
| titleOfInvention |
Methods and kits for linking polymorphic sequences to expanded repeat mutations |
| abstract |
Methods and kits are provided for determining which single nucleotide polymorphism ('SNP') variant of an allele of a heterozygous patient is on the same allele as a disease-causing mutation that is at a remote region of the gene's mRNA comprising a) an allele specific reverse transcription reaction using an allele specific primer which recognizes one SNP variant, wherein further the 3' end of the primer is positioned at the SNP nucleotide position, and b) analysis of the resulting cDNA product from the reverse transcription reaction at the region of the mutation to determine the presence or absence of the mutation on this allele specific cDNA product, wherein the allele specific primer is shorter than about 20 nucleotides. |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9157120-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11732261-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3321361-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11236335-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2009135322-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8957040-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9006198-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3208347-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10202599-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2009244013-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3561060-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3628750-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011097643-A1 |
| priorityDate |
2007-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |