Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_assertion> ?p ?o ?g. }
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- NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_assertion type Assertion NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_head.
- NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_assertion description "[Huntington disease (HD) is a devastating neurologic disorder that is characterized by abnormal expansion of a CAG nt repeat in the first exon of the huntingtin (htt) gene, producing a mutant protein with an elongated polyglutamine stretch.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_provenance.
- NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_assertion evidence source_evidence_literature NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_provenance.
- NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_assertion SIO_000772 15737634 NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_provenance.
- NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_assertion wasDerivedFrom befree-20140225 NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_provenance.
- NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_assertion wasGeneratedBy ECO_0000203 NP477585.RABG35iZaO_8rDf_kmENoCr9CELWl-LGs1cQDzqG-TGls130_provenance.