Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance.
- NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_assertion description "[In a case-control sample that has shown the well established associations between AMD and variants in CFH, CFB and C3 there was absence of association with SNPs in CFP, CD46, CD55 and CD59.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance.
- NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_assertion evidence source_evidence_literature NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance.
- NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_assertion SIO_000772 22024702 NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance.
- NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_assertion wasDerivedFrom befree-20140225 NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance.
- NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_assertion wasGeneratedBy ECO_0000203 NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance.