Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion description "[Ataxia with vitamin E deficiency (AVED), or familial isolated vitamin E deficiency, is a rare autosomal recessive neurodegenerative disease characterized clinically by symptoms with often striking resemblance to those of Friedreich ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion evidence source_evidence_literature NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion SIO_000772 9463307 NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion wasDerivedFrom befree-20140225 NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_assertion wasGeneratedBy ECO_0000203 NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP580634.RA7spHilyIAyxjkt_sntKryZ2jMkxVVRhuKz6i-AcJPuE130_provenance.