Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_provenance.
- NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_assertion description "[To identify suspected RDS mutations in families in which different people have been identified with either generalised retinal dystrophy or macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_provenance.
- NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_assertion evidence source_evidence_literature NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_provenance.
- NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_assertion SIO_000772 16916875 NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_provenance.
- NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_assertion wasDerivedFrom befree-20140225 NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_provenance.
- NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_assertion wasGeneratedBy ECO_0000203 NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP382350.RA8sZxuc7Es5LPSuvyf2anHEZDr8k6F_PAOxqQVIqjGoE130_provenance.