Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_provenance.
- NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_assertion description "[Our findings suggested common genetic changes in IFNAR1 may influence HCC risk, likely through miR-1231-mediated regulation, which is possibly involved in the pathogenesis of HBV related HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_provenance.
- NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_assertion evidence source_evidence_literature NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_provenance.
- NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_assertion SIO_000772 22824466 NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_provenance.
- NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_assertion wasDerivedFrom befree-2016 NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_provenance.
- NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_assertion wasGeneratedBy ECO_0000203 NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_provenance.
- befree-2016 importedOn "2016-02-19" NP999627.RAbm4sn-snhvY1zr-e0c52zZKSq2pra9pCmUroxm2niIM130_provenance.