Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_provenance.
- NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_assertion description "[Specific variants of the MC1R gene have been demonstrated to confer an increase in melanoma risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_provenance.
- NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_assertion evidence source_evidence_literature NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_provenance.
- NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_assertion SIO_000772 16759158 NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_provenance.
- NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_assertion wasDerivedFrom befree-2016 NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_provenance.
- NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_assertion wasGeneratedBy ECO_0000203 NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_provenance.
- befree-2016 importedOn "2016-02-19" NP553465.RAc_3bnd3JaPwnl8-W-Eql5wegaLKwXFI-TlAc1lU1SxE130_provenance.