Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_provenance.
- NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_assertion description "[Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot-Marie-Tooth disease family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_provenance.
- NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_assertion evidence source_evidence_literature NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_provenance.
- NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_assertion SIO_000772 15947997 NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_provenance.
- NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_assertion wasDerivedFrom befree-20140225 NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_provenance.
- NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_assertion wasGeneratedBy ECO_0000203 NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP188942.RAUxf-AlBBlcRcPLNzfGr0eW54kQDwK6DAwbqUs0CA8Tk130_provenance.