Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion description "[These results indicate a significant modification of the phenotype of FH with defective LDLR allele by EPHX2-287Arg variation in our studied kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion evidence source_evidence_literature NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion SIO_000772 14673705 NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion wasDerivedFrom befree-2016 NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_assertion wasGeneratedBy ECO_0000203 NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.
- befree-2016 importedOn "2016-02-19" NP424419.RAAPj39GXOImH8xvHbk2LYKj3B-tvoCIVC7_wTSFvjat0130_provenance.