Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance.
- NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_assertion wasGeneratedBy ECO_0000203 NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance.
- NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_assertion wasDerivedFrom befree-20150227 NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance.
- NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_assertion SIO_000772 11331249 NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance.
- NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_assertion evidence source_evidence_literature NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance.
- NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_assertion description "[RE repeats encoded (RERE) was identified recently as a protein with high homology to the atrophin-1 protein, which appears to be causal in the hereditary neurodegenerative disorder termed dentatorubral-pallidoluysian atrophy (DRPLA) caused by an abnormal glutamine expansion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361249.RAB_hUZp56UkIlFMZ1RkYcyaMHSzM-5vOdr0eYFEOGxPw130_provenance.