Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_provenance.
- NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_assertion description "[We initially conducted a comparative genetic analysis of neovascular AMD and PCV, genotyping the ARMS2 A69S variant in 181 subjects with neovascular AMD, 198 subjects with PCV, and 203 controls in a Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_provenance.
- NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_assertion evidence source_evidence_literature NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_provenance.
- NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_assertion SIO_000772 22219653 NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_provenance.
- NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_assertion wasDerivedFrom befree-20140225 NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_provenance.
- NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_assertion wasGeneratedBy ECO_0000203 NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP579656.RA9za212thdhu0IV-TqrYdR7G-iTDojs5KZA9Ym2KDX7k130_provenance.