Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_provenance.
- NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_assertion description "[Among the 60 patients with sporadic ataxias in the present series, 3 (5.0%) were found to harbor SCA3 mutations, whereas none were found to harbor SCA6 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_provenance.
- NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_assertion evidence source_evidence_literature NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_provenance.
- NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_assertion SIO_000772 15979648 NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_provenance.
- NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_assertion wasDerivedFrom befree-20150227 NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_provenance.
- NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_assertion wasGeneratedBy ECO_0000203 NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP557296.RAF9-dSH0Y1cKPOt0K4vhbCHBv6L0AeXQ6Oya232pgTnE130_provenance.