Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_provenance.
- NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_assertion description "[Despite the clinical diversity and atypical laboratory findings seen in familial CJD with the codon 200 mutation, these neuroimaging studies suggest that common regional distributions and a common pathogenesis might underlie the clinical progression both in sporadic CJD and in familial CJD with the codon 200 mutation in the prion protein gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_provenance.
- NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_assertion evidence source_evidence_literature NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_provenance.
- NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_assertion SIO_000772 15850581 NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_provenance.
- NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_assertion wasDerivedFrom befree-2016 NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_provenance.
- NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_assertion wasGeneratedBy ECO_0000203 NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_provenance.
- befree-2016 importedOn "2016-02-19" NP491359.RArOgzj_uQycnW3aun2d-XYusJP9a4Nzz3VZoA3N9CuOU130_provenance.