Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_provenance.
- NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_assertion description "[However, allele sizes within the SCA8 proposed pathogenic range have been reported in patients with ataxia of unknown etiology, in individuals from pedigrees with other SCA or Friedreich's ataxia, and in patients with Alzheimer's disease, schizophrenia or parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_provenance.
- NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_assertion evidence source_evidence_literature NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_provenance.
- NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_assertion SIO_000772 18708037 NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_provenance.
- NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_assertion wasDerivedFrom befree-20150227 NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_provenance.
- NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_assertion wasGeneratedBy ECO_0000203 NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP923776.RAmQ4qpLhFVwCpmKK_1uvFBriSLFt1UScYN02octXjno4130_provenance.