Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_provenance.
- NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_assertion description "[In AD cases, a SNP within the same haplotype was associated with reduced RNASEN mRNA expression (P=0.013) and with miR expression changes (global P=0.007) of miRs known to be associated with cancer (e.g., let-7 family, miR-21, miR-25, miR-126 and miR15a).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_provenance.
- NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_assertion evidence source_evidence_literature NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_provenance.
- NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_assertion SIO_000772 21102586 NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_provenance.
- NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_assertion wasDerivedFrom befree-2016 NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_provenance.
- NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_assertion wasGeneratedBy ECO_0000203 NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_provenance.
- befree-2016 importedOn "2016-02-19" NP854232.RA5gEllvFUDYhffAWmzacHyWVRM_vpFBbOW3Dac7a4Exs130_provenance.