Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_provenance.
- NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_assertion wasGeneratedBy ECO_0000203 NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_provenance.
- NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_assertion wasDerivedFrom lhgdn-20090331 NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_provenance.
- NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_assertion SIO_000772 17072629 NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_provenance.
- NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_assertion evidence source_evidence_literature NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_provenance.
- NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_assertion description "[Melanoma risk increased with the number of variant MC1R alleles carried by an individual]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182049.RAUOYqvkZVp7GtTntD44YBMHIJ-FuaR-824XHuY_p7Fhg130_provenance.