Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_provenance.
- NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_assertion description "[Huntington disease is a neurodegenerative disorder caused by a CAG repeat amplification in the gene huntingtin (HTT) that is reflected by a polyglutamine expansion in the Htt protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_provenance.
- NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_assertion evidence source_evidence_literature NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_provenance.
- NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_assertion SIO_000772 22556411 NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_provenance.
- NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_assertion wasDerivedFrom befree-20150227 NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_provenance.
- NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_assertion wasGeneratedBy ECO_0000203 NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP699299.RAsUzN1vOPyauKY_yzBQuSxohsLCzqLfqf2b9NMuKGZfI130_provenance.