Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_provenance.
- NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_assertion description "[The highest odds ratios (ORs) for the associations were observed between the homozygous variant genotype XRCC1 Gln399Gln and the risk of glioma (OR = 1.32; 95% confidence interval, CI, 0.97-1.81), glioblastoma (OR = 1.48; 95% CI, 0.98-2.24), and meningioma (OR = 1.34; 95% CI, 0.96-1.86).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_provenance.
- NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_assertion evidence source_evidence_literature NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_provenance.
- NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_assertion SIO_000772 18330515 NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_provenance.
- NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_assertion wasDerivedFrom befree-20140225 NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_provenance.
- NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_assertion wasGeneratedBy ECO_0000203 NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP476172.RAt-meHwWcLxncmKRUq4GPOgddDCHwSL4Uk5g24-p7aDE130_provenance.