Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_provenance.
- NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_assertion description "[To assess the role of MC1R variants in uveal melanoma, we have analysed a cohort of 350 patients for the changes within the major region of the gene displaying sequence variation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_provenance.
- NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_assertion evidence source_evidence_literature NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_provenance.
- NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_assertion SIO_000772 14612910 NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_provenance.
- NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_assertion wasDerivedFrom befree-20140225 NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_provenance.
- NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_assertion wasGeneratedBy ECO_0000203 NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP665676.RA417hV8cE1t9XKcdoSI7erl6AWshK6uBfkPx4yTcEGGU130_provenance.