Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_provenance.
- NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_assertion wasGeneratedBy ECO_0000203 NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_provenance.
- NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_assertion wasDerivedFrom befree-20140225 NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_provenance.
- NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_assertion SIO_000772 11591855 NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_provenance.
- NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_assertion evidence source_evidence_literature NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_provenance.
- NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_assertion description "[The authors found allele sizes within the proposed pathogenic range in three patients with ataxia of unknown etiology, in two individuals from pedigrees with either SCA2 or Friedreich's ataxia, and in two patients with Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_provenance.
- befree-20140225 importedOn "2014-02-25" NP232313.RAQJBXJdSBDqOTFfUUwC8Jqjth5BvDy-siWxQsVUrgTog130_provenance.