Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_provenance.
- NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_assertion description "[A genome-wide association study (GWAS) identified significant association between variants in MEIS1, BTBD9, and MAP2K5/SKOR1 and restless legs syndrome (RLS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_provenance.
- NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_assertion evidence source_evidence_literature NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_provenance.
- NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_assertion SIO_000772 21925394 NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_provenance.
- NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_assertion wasDerivedFrom befree-20140225 NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_provenance.
- NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_assertion wasGeneratedBy ECO_0000203 NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP555130.RA2eJsCId2iNFXQxGUeMzdnMgEGLtbOe_IaF_rlgrYL-g130_provenance.