Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_assertion> ?p ?o ?g. }
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- NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_assertion type Assertion NP480892.RAuD1Su9S4SGcYUrf5ijE-9ZYDg7J-atdEH2Jqe8oTLeA130_head.
- 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.