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- source_evidence_literature type ECO_0000212 NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_provenance.
- NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_assertion description "[WRN was originally identified as a gene responsible for Werner syndrome (WS; Progeria of Adults).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_provenance.
- NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_assertion evidence source_evidence_literature NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_provenance.
- NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_assertion SIO_000772 10984715 NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_provenance.
- NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_assertion wasDerivedFrom befree-2016 NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_provenance.
- NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_assertion wasGeneratedBy ECO_0000203 NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_provenance.
- befree-2016 importedOn "2016-02-19" NP294941.RAOhrgHUfjUg920Q_mwZ0p2v7cI7-pw6lUxFg1qs2Z770130_provenance.