Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_provenance.
- NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_assertion description "[We have screened seven genes known to reside in or very close to this overlap consensus region, UBE4B/UFD2, KIF1B, DFFA, PGD, CORT, PEX14, and ICAT, for coding mutations in NBL tumor DNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_provenance.
- NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_assertion evidence source_evidence_literature NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_provenance.
- NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_assertion SIO_000772 12700669 NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_provenance.
- NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_assertion wasDerivedFrom befree-20140225 NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_provenance.
- NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_assertion wasGeneratedBy ECO_0000203 NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477728.RAOHL6LP01jEHudYFz2anLZwVCHii_6Dg3qvyRz2bN7Ig130_provenance.