Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_provenance.
- NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_assertion description "[In over 50% of cases the causative gene is CACNA1A (FHM1), which in some cases produces a phenotype with cerebellar signs, including ataxia and nystagmus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_provenance.
- NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_assertion evidence source_evidence_literature NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_provenance.
- NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_assertion SIO_000772 15459825 NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_provenance.
- NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_assertion wasDerivedFrom befree-2016 NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_provenance.
- NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_assertion wasGeneratedBy ECO_0000203 NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_provenance.
- befree-2016 importedOn "2016-02-19" NP462806.RA5NE3XLfbwHXgILHa7FYRFmF9pSjsZ8Zo-g3DiYygHZM130_provenance.