Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance.
- befree-20150227 importedOn "2015-02-27" NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance.
- NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_assertion wasGeneratedBy ECO_0000203 NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance.
- NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_assertion wasDerivedFrom befree-20150227 NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance.
- NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_assertion SIO_000772 21035104 NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance.
- NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_assertion evidence source_evidence_literature NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance.
- NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_assertion description "[PDYN mutations are identified in a small subset of ataxia families, indicating that SCA23 is an infrequent SCA type (∼0.5%) in the Netherlands and suggesting further genetic SCA heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance.