Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance.
- NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_assertion description "[Using exome sequencing, we identified recurrent somatic mutations in EIF1AX and SF3B1, specifically occurring in uveal melanomas with disomy 3, which rarely metastasize.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance.
- NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_assertion evidence source_evidence_literature NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance.
- NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_assertion SIO_000772 23793026 NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance.
- NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_assertion wasDerivedFrom befree-20140225 NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance.
- NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_assertion wasGeneratedBy ECO_0000203 NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP213922.RADWn8xEwIi6HJszevgkFNQ_g2w1rCjsrNnQQ2VfM0imM130_provenance.