Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_provenance.
- NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_assertion description "[A gene dosage effect was noted, with significantly increased melanoma risk being observed in subjects with at least two variants whether when all variants are pooled (OR=4.8, 95% CI: 2.0-11.2; p=0.002 after Bonferroni correction) or when red hair colour (RHC) variants and non-RHC variants are distinguished (OR=7.6, 95% CI: 2.8-20.3; p=0.0004 after Bonferroni correction).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_provenance.
- NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_assertion evidence source_evidence_literature NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_provenance.
- NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_assertion SIO_000772 19269164 NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_provenance.
- NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_assertion wasDerivedFrom befree-20140225 NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_provenance.
- NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_assertion wasGeneratedBy ECO_0000203 NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP875131.RADXgKp9Mgqafgj211R4MtLn8131gEw67Dtckpbhv4Zo4130_provenance.