Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_provenance.
- befree-2016 importedOn "2016-02-19" NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_provenance.
- NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_assertion wasGeneratedBy ECO_0000203 NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_provenance.
- NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_assertion wasDerivedFrom befree-2016 NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_provenance.
- NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_assertion SIO_000772 22004887 NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_provenance.
- NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_assertion evidence source_evidence_literature NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_provenance.
- NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_assertion description "[This report provide a wide spectrum of USH2A mutations and clinical features, including atypical Usher syndrome phenotypes resembling Usher syndrome type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931596.RAvcm0vZP5LwFcGuDM10A4NKjiaPiVuUD1WC6GY9Dfy5U130_provenance.