Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_provenance.
- befree-2016 importedOn "2016-02-19" NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_provenance.
- NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_assertion wasGeneratedBy ECO_0000203 NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_provenance.
- NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_assertion wasDerivedFrom befree-2016 NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_provenance.
- NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_assertion SIO_000772 11252306 NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_provenance.
- NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_assertion evidence source_evidence_literature NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_provenance.
- NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_assertion description "[Defects in polycystin-2, a ubiquitous transmembrane glycoprotein of unknown function, is a major cause of autosomal dominant polycystic kidney disease (ADPKD), whose manifestation entails the development of fluid-filled cysts in target organs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311281.RADc6I_FqxXIA0r2Z8UI8ajFxVfKBfNyMnwycM1d0v32M130_provenance.