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- source_evidence_literature type ECO_0000212 NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_provenance.
- NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_assertion description "[This gene, which encodes a member of the potassium channel, voltage-gated, shaker-related subfamily, has not been previously described as a cause of disease in humans, but mutations of the orthologous gene in mice (Kcna2) are known to cause both ataxia and convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_provenance.
- NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_assertion evidence source_evidence_literature NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_provenance.
- NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_assertion SIO_000772 25477152 NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_provenance.
- NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_assertion wasDerivedFrom befree-2016 NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_provenance.
- NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_assertion wasGeneratedBy ECO_0000203 NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245028.RAx-Sfw3vVl_5LJ5B3QuuD71XScl1a4bgbkNITKupj1fA130_provenance.