Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_provenance.
- NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_assertion description "[Mutation analyses for SCA1, 2, 3, 6, 7, 8, 10, 12, 17, and DRPLA and frataxin genes were performed for 251 unrelated Finnish patients who presented with progressive ataxia disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_provenance.
- NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_assertion evidence source_evidence_literature NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_provenance.
- NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_assertion SIO_000772 15691283 NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_provenance.
- NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_assertion wasDerivedFrom befree-20150227 NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_provenance.
- NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_assertion wasGeneratedBy ECO_0000203 NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681577.RA-tmdwF3YOr2eJXfiliwqHSRIQQqa9czvLcY3MrdLdyU130_provenance.