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- source_evidence_literature type ECO_0000212 NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_provenance.
- NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_assertion description "[Huntington disease (HD) is an inherited neurological disorder caused by a polyglutamine expansion in the protein huntingtin and is characterized by selective neurodegeneration that preferentially occurs in striatal medium spiny neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_provenance.
- NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_assertion evidence source_evidence_literature NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_provenance.
- NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_assertion SIO_000772 20018729 NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_provenance.
- NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_assertion wasDerivedFrom befree-20140225 NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_provenance.
- NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_assertion wasGeneratedBy ECO_0000203 NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697081.RA9h1bTwg3DvHfjvfp8ugWEuTqu-ug4BpHD8E4dcYI49A130_provenance.