Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_provenance.
- NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_assertion description "[The rare CX3CR1 alleles were associated with an increased risk of BI and with reduced frequency of cardiovascular history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_provenance.
- NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_assertion evidence source_evidence_literature NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_provenance.
- NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_assertion SIO_000772 15681302 NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_provenance.
- NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_assertion wasDerivedFrom befree-2016 NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_provenance.
- NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_assertion wasGeneratedBy ECO_0000203 NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_provenance.
- befree-2016 importedOn "2016-02-19" NP478561.RAhP30Mc94vpEffnVgbS4E5O_9U-ck6EiYbyy58o_mBr4130_provenance.