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- source_evidence_literature type ECO_0000212 NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- befree-2016 importedOn "2016-02-19" NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion wasGeneratedBy ECO_0000203 NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion wasDerivedFrom befree-2016 NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion SIO_000772 20075015 NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion evidence source_evidence_literature NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.
- NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_assertion description "[Mutations in the WRN gene are the causative factor of Werner syndrome (WS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787168.RAMQCT1K-AgTMDL95C41711VFscnwMB5EsVLfD6hSCOA4130_provenance.