Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance.
- NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_assertion description "[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance.
- NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_assertion evidence source_evidence_literature NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance.
- NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_assertion SIO_000772 17903303 NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance.
- NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_assertion wasDerivedFrom gad-20130706 NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance.
- NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_assertion wasGeneratedBy ECO_0000203 NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP93986.RArN2p9CHsLzoEOImaP-vPrgrFrHVbYgLKqeaH_bWQHBE130_provenance.