Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_provenance.
- NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_assertion wasGeneratedBy ECO_0000203 NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_provenance.
- NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_assertion wasDerivedFrom lhgdn-20090331 NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_provenance.
- NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_assertion SIO_000772 15733840 NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_provenance.
- NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_assertion evidence source_evidence_literature NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_provenance.
- NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_assertion description "[a novel pathway in which Nbs1 may recruit Werner syndrome protein to the site of DNA double strand breaks in an ATM-dependent manner ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209455.RA_peFZIJ76l3dHFasQ9mPQYxV-P-FDMbZDkbZOTElIgo130_provenance.