Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_provenance.
- befree-2016 importedOn "2016-02-19" NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_provenance.
- NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_assertion wasGeneratedBy ECO_0000203 NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_provenance.
- NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_assertion wasDerivedFrom befree-2016 NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_provenance.
- NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_assertion SIO_000772 21513696 NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_provenance.
- NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_assertion evidence source_evidence_literature NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_provenance.
- NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_assertion description "[Huntington disease (HD) is a neurodegenerative disorder caused by expansion of CAG trinucleotide repeats, leading to an elongated polyglutamine sequence (polyQ) in the huntingtin protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889036.RA0T_r-vth93pv2I55kdeRjMN0ksoYkquZkFwFPzdfS4U130_provenance.