Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_provenance.
- NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_assertion description "[We found suggestive linkage of the BFNC phenotype to the 20q13-EBN1 locus (lod score, 2.03) and an intronic mutation IVS14-6 C>A in KCNQ2 segregating with the trait in all affected members, but absent in 100 unrelated control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_provenance.
- NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_assertion evidence source_evidence_literature NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_provenance.
- NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_assertion SIO_000772 16686649 NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_provenance.
- NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_assertion wasDerivedFrom befree-20150227 NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_provenance.
- NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_assertion wasGeneratedBy ECO_0000203 NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP314262.RAA3GHE85UPozRHDmvVsYulXJvrI7afhCEQYXOtczSxAo130_provenance.