Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_provenance.
- NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_assertion description "[A pronounced lack of Frataxin causes Friedreich's Ataxia, which is a human neurodegenerative and hereditary disease mainly affecting the equilibrium, coordination, muscles and heart.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_provenance.
- NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_assertion evidence source_evidence_literature NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_provenance.
- NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_assertion SIO_000772 23463383 NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_provenance.
- NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_assertion wasDerivedFrom befree-20140225 NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_provenance.
- NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_assertion wasGeneratedBy ECO_0000203 NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_provenance.
- befree-20140225 importedOn "2014-02-25" NP523263.RA2CbGBekxgldkYbX9Vi7J1RFgFb7OD1xZjzbRWDCy4Ls130_provenance.