Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_provenance.
- NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_assertion description "[Hypomorphic mutations in the NBS1 and MRE11 genes lead to two other genomic instability disorders: the Nijmegen breakage syndrome (NBS) and A-T like disease (A-TLD), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_provenance.
- NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_assertion evidence source_evidence_literature NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_provenance.
- NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_assertion SIO_000772 14532133 NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_provenance.
- NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_assertion wasDerivedFrom befree-20140225 NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_provenance.
- NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_assertion wasGeneratedBy ECO_0000203 NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP157162.RAUYG85UBLa0ekxsuUFoUEL6hyTgVkeYWpz4dP1n9v0ZM130_provenance.