Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_provenance.
- NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_assertion description "[Here, we provide an overview of current knowledge on SCN5A mutations associated with sodium channel overlap syndromes and discuss a possible role for modifiers in determining disease expressivity in the individual patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_provenance.
- NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_assertion evidence source_evidence_literature NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_provenance.
- NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_assertion SIO_000772 18436145 NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_provenance.
- NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_assertion wasDerivedFrom befree-20140225 NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_provenance.
- NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_assertion wasGeneratedBy ECO_0000203 NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP522637.RA2j9EImaLAGxkIGSye007t0DmrnB_MSmZR4MsN4MLXP4130_provenance.