Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_provenance.
- NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_assertion description "[The SNP1350T/C variant in the TLR2 gene showed a lower frequency in the AMI patient group than in the control group (P = 0.033).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_provenance.
- NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_assertion evidence source_evidence_literature NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_provenance.
- NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_assertion SIO_000772 22229967 NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_provenance.
- NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_assertion wasDerivedFrom befree-20140225 NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_provenance.
- NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_assertion wasGeneratedBy ECO_0000203 NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_provenance.