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- source_evidence_literature type ECO_0000212 NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_provenance.
- NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_assertion description "[Finally, paroxysmal exertion-induced dystonia (DYT18, GLUT1 deficiency) is caused by mutations in the SLC2A1 gene (DYT9 and DYT18).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_provenance.
- NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_assertion evidence source_evidence_literature NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_provenance.
- NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_assertion SIO_000772 22166420 NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_provenance.
- NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_assertion wasDerivedFrom befree-20150227 NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_provenance.
- NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_assertion wasGeneratedBy ECO_0000203 NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP329341.RAA-yLIc9QlErnapnau-U52g_8ztmijtRVSFnOgEbIZqg130_provenance.