Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_provenance.
- NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_assertion description "[Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_provenance.
- NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_assertion evidence source_evidence_literature NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_provenance.
- NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_assertion SIO_000772 23793026 NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_provenance.
- NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_assertion wasDerivedFrom befree-20140225 NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_provenance.
- NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_assertion wasGeneratedBy ECO_0000203 NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP291720.RAscc8z3pbcC58QPchx7CYUUpKrLYNzhUogSKKLBKnljM130_provenance.