Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_provenance.
- NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_assertion description "[Our meta-analysis provides substantial evidence that the ARMS2 A69S variant confers a significantly higher risk of neovascular AMD than PCV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_provenance.
- NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_assertion evidence source_evidence_literature NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_provenance.
- NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_assertion SIO_000772 22219653 NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_provenance.
- NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_assertion wasDerivedFrom befree-2016 NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_provenance.
- NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_assertion wasGeneratedBy ECO_0000203 NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_provenance.
- befree-2016 importedOn "2016-02-19" NP951028.RA0U3JFLP4t0boJURltN6qjnqtUrG7eGNkaZfuXvr1HjY130_provenance.