Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_provenance.
- NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_assertion description "[The SCA12 mutation as a rare cause of spinocerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_provenance.
- NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_assertion evidence source_evidence_literature NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_provenance.
- NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_assertion SIO_000772 11708992 NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_provenance.
- NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_assertion wasDerivedFrom befree-20140225 NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_provenance.
- NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_assertion wasGeneratedBy ECO_0000203 NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP696869.RAyyjN63oBOvV-tIRIujnfDizj1vZp2KnNBzt8oD-dsiA130_provenance.