Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_provenance.
- NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_assertion description "[Eight SNPs showed significant associations with the risk of SPT/recurrence, with the most significant one of rs2179653, which is located in the 5'-flanking region of RGS2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_provenance.
- NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_assertion evidence source_evidence_literature NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_provenance.
- NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_assertion SIO_000772 20627871 NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_provenance.
- NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_assertion wasDerivedFrom befree-20140225 NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_provenance.
- NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_assertion wasGeneratedBy ECO_0000203 NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP267893.RA5h4Iv_wrxA0dYCzn76NXfE3K695EZlx4f19h_-LSqIs130_provenance.