Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion description "[Three patients with AOA1 were identified in an APTX mutation screening on 28 Southern Italian patients with progressive ataxia and peripheral neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion evidence source_evidence_literature NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion SIO_000772 15596775 NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion wasDerivedFrom befree-2016 NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_assertion wasGeneratedBy ECO_0000203 NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.
- befree-2016 importedOn "2016-02-19" NP472613.RA1h788BK9BUkj34jQDd0LWJScsLxmEdWuynmKYOopMRA130_provenance.