Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_provenance.
- befree-2016 importedOn "2016-02-19" NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_provenance.
- NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_assertion wasGeneratedBy ECO_0000203 NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_provenance.
- NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_assertion wasDerivedFrom befree-2016 NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_provenance.
- NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_assertion SIO_000772 21717286 NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_provenance.
- NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_assertion evidence source_evidence_literature NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_provenance.
- NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_assertion description "[A total of 184 individuals were eligible for presymptomatic testing due to a risk for spinocerebellar ataxia (SCA) - SCA3 (80%), Huntington's disease (11.9%), familial amyloidotic neuropathy (4.3%), SCA1, SCA2, SCA6, or SCA7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP906050.RAPtLa_LZpkB2foR1UZBsK8qRAdA-o0ujdo6kYLQzxQhk130_provenance.