Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_provenance.
- NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_assertion wasGeneratedBy ECO_0000203 NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_provenance.
- NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_assertion wasDerivedFrom befree-20150227 NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_provenance.
- NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_assertion SIO_000772 12383275 NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_provenance.
- NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_assertion evidence source_evidence_literature NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_provenance.
- NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_assertion description "[Mutation of a voltage-gated K+-channel gene can cause partial seizures associated with periodic ataxia type 1 and some forms of juvenile myoclonic epilepsy can result from mutations of a Ca2+ channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521559.RAg5Jrsoeo30rDGcENtiAFw0sWW29cZJ6B-y89tI1g2SY130_provenance.