Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_provenance.
- NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_assertion description "[Spinocerebellar ataxia type 31 (SCA31), is a recently defined subtype of autosomal dominant cerebellar ataxia (ADCA) characterized by late-onset pure cerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_provenance.
- NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_assertion evidence source_evidence_literature NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_provenance.
- NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_assertion SIO_000772 22353852 NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_provenance.
- NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_assertion wasDerivedFrom befree-20140225 NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_provenance.
- NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_assertion wasGeneratedBy ECO_0000203 NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP485471.RAFDrYsNpKo7zfyhCK-iOyH02bbjhN2A1XFc2rPn-DUDU130_provenance.