Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_provenance.
- NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_assertion description "[Within this region, we defined a 42-SNP haplotype that was associated with significantly increased risk of ALS (p=7�47�10(-33) when people with familial ALS were compared with controls, odds ratio 21�0, 95% CI 11�2-39�1) and which overlapped with an association locus recently reported for frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_provenance.
- NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_assertion evidence source_evidence_literature NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_provenance.
- NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_assertion SIO_000772 20801718 NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_provenance.
- NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_assertion wasDerivedFrom befree-20140225 NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_provenance.
- NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_assertion wasGeneratedBy ECO_0000203 NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP201905.RAChK523ERqyYlYCmPEVcCQZyjGtAdy_DQ5K3TPmOCDLE130_provenance.