Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance.
- NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_assertion description "[GSS, associated with a missense mutation at codon 102 of the prion protein (PrP) gene (GSS102), is a hereditary disorder that presents with progressive ataxia and dementia, and is characterized by the loss of deep tendon reflexes and painful dysesthesias of the legs in its early stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance.
- NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_assertion evidence source_evidence_literature NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance.
- NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_assertion SIO_000772 9932941 NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance.
- NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_assertion wasDerivedFrom befree-20140225 NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance.
- NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_assertion wasGeneratedBy ECO_0000203 NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP824827.RA361f8cvPWv_e8oM5C0Xhn_7URziftw7-s4q7c1M-Lrc130_provenance.