Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_provenance.
- NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_assertion description "[We have mapped EFEMP2 to 11q13, in an area where several retinopathies have been genetically linked.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_provenance.
- NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_assertion evidence source_evidence_literature NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_provenance.
- NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_assertion SIO_000772 10982184 NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_provenance.
- NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_assertion wasDerivedFrom befree-2016 NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_provenance.
- NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_assertion wasGeneratedBy ECO_0000203 NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_provenance.
- befree-2016 importedOn "2016-02-19" NP294747.RAXOPVGz5YO7ny-jlxpkb_AOBKFu5PLRbZ_pJ4eF8v8Us130_provenance.