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- source_evidence_literature type ECO_0000212 NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_provenance.
- NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_assertion description "[Coding SNPs in TLR3 (rs3775291) and TLR7 (rs179008) showed association with AMD in one group (P = 0.01 and P = 0.02, respectively) before correction for multiple testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_provenance.
- NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_assertion evidence source_evidence_literature NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_provenance.
- NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_assertion SIO_000772 18385087 NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_provenance.
- NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_assertion wasDerivedFrom befree-20150227 NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_provenance.
- NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_assertion wasGeneratedBy ECO_0000203 NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP903961.RAhpei_1dw6z1WcQBWO0lpPZ9VT0N6z9o_YHYlsityYRE130_provenance.