Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance.
- NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_assertion description "[PRRT2 mutations are common in patients with PKD and are significantly associated with an earlier age at onset, longer duration of attacks, a complicated form of PKD, combined phenotypes of dystonia and chorea, and a tendency for a family history of PKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance.
- NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_assertion evidence source_evidence_literature NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance.
- NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_assertion SIO_000772 26446061 NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance.
- NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_assertion wasDerivedFrom befree-2016 NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance.
- NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_assertion wasGeneratedBy ECO_0000203 NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1294753.RAXuOJ9Ht3uQkuIzREwIXdetNVG_nOFOeCVx7_pV-rsfA130_provenance.