Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_provenance.
- NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_assertion description "[Protein truncation mutations in ELOVL4 have been identified in patients with autosomal dominant Stargardt-like macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_provenance.
- NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_assertion evidence source_evidence_literature NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_provenance.
- NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_assertion SIO_000772 16036915 NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_provenance.
- NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_assertion wasDerivedFrom befree-2016 NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_provenance.
- NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_assertion wasGeneratedBy ECO_0000203 NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_provenance.
- befree-2016 importedOn "2016-02-19" NP505282.RATDcyQTNP8prQ8Tl7mup3ULtl4Kvb3yvzREv6ENQOhfw130_provenance.