Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_provenance.
- befree-20150227 importedOn "2015-02-27" NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_provenance.
- NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_assertion wasGeneratedBy ECO_0000203 NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_provenance.
- NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_assertion wasDerivedFrom befree-20150227 NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_provenance.
- NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_assertion SIO_000772 12116198 NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_provenance.
- NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_assertion evidence source_evidence_literature NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_provenance.
- NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_assertion description "[The frequency of SCA subtypes in autosomal dominant group was: 1) 5.5% for SCA1; 2) 2.4% for SCA2; 3) 27.6% for MJD/SCA3; 4) 25.5% for SCA6; 5) 0.3% for SCA17; and 6) 7.3% for DRPLA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557466.RADxW9UgVumuOozh4ZARP2vemEa5QMgT9g9ngTgCBD2Ak130_provenance.