Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_provenance.
- NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_assertion description "[Huntington's disease (HD) is a hereditary neurodegenerative disorder resulting from the expansion of a polyglutamine tract in the huntingtin protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_provenance.
- NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_assertion evidence source_evidence_literature NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_provenance.
- NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_assertion SIO_000772 22399227 NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_provenance.
- NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_assertion wasDerivedFrom befree-20140225 NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_provenance.
- NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_assertion wasGeneratedBy ECO_0000203 NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP426815.RAiDldm_2jBLkGuGXj2CC-SgEYSkSOtTnbzZDeNIYEBWY130_provenance.