Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_provenance.
- NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_assertion description "[These results suggest that SCA may be occasionally caused by the SCA1 mutation and rarely caused by the DRPLA mutation and that, to date, the MJD mutation seems to be the most common cause of dominantly inherited SCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_provenance.
- NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_assertion evidence source_evidence_literature NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_provenance.
- NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_assertion SIO_000772 8559378 NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_provenance.
- NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_assertion wasDerivedFrom befree-20150227 NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_provenance.
- NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_assertion wasGeneratedBy ECO_0000203 NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_provenance.
- befree-20150227 importedOn "2015-02-27" NP681519.RAYL7X7cluW7QV4cxVCaaIH5RFh69koG9xXsXX4rq_0Ak130_provenance.