Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_provenance.
- NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_assertion description "[Molecular genetic testing allowed us to assign 202 ADCA-I patients to one of the following subgroups: spinocerebellar ataxia type I (SCAI, n = 36), SCA2 (n = 56) and SCA3 (n = 110).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_provenance.
- NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_assertion evidence source_evidence_literature NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_provenance.
- NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_assertion SIO_000772 9577387 NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_provenance.
- NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_assertion wasDerivedFrom befree-20140225 NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_provenance.
- NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_assertion wasGeneratedBy ECO_0000203 NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP775367.RAh5Sc1O9iQ0vqqZW_v9BHBXdPEIRB-0DJPH8BXJeWLeg130_provenance.