Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_provenance.
- NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_assertion description "[Genetic susceptibility to CAD may be determined by polymorphic variants of genes encoding isoforms involved in the processes important in the pathogenesis of atherosclerosis, including lipids disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_provenance.
- NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_assertion evidence source_evidence_literature NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_provenance.
- NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_assertion SIO_000772 18219093 NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_provenance.
- NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_assertion wasDerivedFrom befree-2016 NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_provenance.
- NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_assertion wasGeneratedBy ECO_0000203 NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_provenance.
- befree-2016 importedOn "2016-02-19" NP651615.RA380B80AOMRV9FqaDi5NvXeTa3WHWGn-em6D_Lmd_rrs130_provenance.