Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_provenance.
- NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_assertion description "[They include at least nine disorders, including Huntington's disease (HD), dentatorubral pallidoluysian atrophy (DRPLA), spinal and bulbar muscular atrophy (SBMA), and the spinocerebellar ataxias SCA1, SCA2, SCA3 (also known as Machado-Joseph disease), SCA6, SCA7, and SCA17.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_provenance.
- NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_assertion evidence source_evidence_literature NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_provenance.
- NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_assertion SIO_000772 17786457 NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_provenance.
- NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_assertion wasDerivedFrom befree-20150227 NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_provenance.
- NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_assertion wasGeneratedBy ECO_0000203 NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681554.RA5NhXwjisZG2s4UHYAB4__9291Q5_GVTjEhrR-Ct__aA130_provenance.