Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance.
- NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_assertion description "[Huntington's disease (HD), spinocerebellar ataxias types 1 and 3 (SCA1, SCA3), and spinobulbar muscular atrophy (SBMA) are caused by CAG/polyglutamine expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance.
- NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_assertion evidence source_evidence_literature NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance.
- NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_assertion SIO_000772 10717003 NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance.
- NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_assertion wasDerivedFrom befree-20140225 NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance.
- NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_assertion wasGeneratedBy ECO_0000203 NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_provenance.