Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion description "[The most common cause of inherited SCA was a mutation at the SCA6 locus (25%), followed by mutation at the SCA1 locus (15%), SCA3 locus (5%) and dentatorubral-pallidoluysian atrophy locus (5%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion evidence source_evidence_literature NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion SIO_000772 11359084 NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion wasDerivedFrom befree-20150227 NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_assertion wasGeneratedBy ECO_0000203 NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681606.RAHL6MBiqBGzc0vpUp5KUiRRVOhjMhnVp6wcM5WX0SYfE130_provenance.