Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_provenance.
- befree-2016 importedOn "2016-02-19" NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_provenance.
- NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_assertion wasGeneratedBy ECO_0000203 NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_provenance.
- NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_assertion wasDerivedFrom befree-2016 NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_provenance.
- NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_assertion SIO_000772 1360045 NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_provenance.
- NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_assertion evidence source_evidence_literature NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_provenance.
- NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_assertion description "[Although most of the PKD1 families were ascertained through clinics treating patients with renal impairment, no non-PKD1 family was identified through this source.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411580.RAgDOhNmzSIix1_Dl6tUo3wBQQw0Ffdnl6MAO5I0EkgF8130_provenance.