Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_assertion> ?p ?o ?g. }
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- NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_assertion type Assertion NP932942.RAeKFH4dUY2KGdqdj8KCvPV7tBm1SsY7e1Uvfzaims1nU130_head.
- 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.