Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion description "[Spinocerebellar ataxia type 6 (SCA6) was recently identified as a form of autosomal dominant spinocerebellar ataxia associated with a small CAG repeat expansion of the gene encoding an alpha 1 A-voltage-dependent calcium channel gene subunit on chromosome 19p13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion evidence source_evidence_literature NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion SIO_000772 10985694 NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion wasDerivedFrom befree-20150227 NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_assertion wasGeneratedBy ECO_0000203 NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP225872.RAdsCnDGaYEMKLoOm208VMsFI1uQMtbCXDW8uG_0Tdyv8130_provenance.