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- source_evidence_literature type ECO_0000212 NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_provenance.
- NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_provenance.
- NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_assertion evidence source_evidence_literature NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_provenance.
- NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_assertion SIO_000772 8737929 NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_provenance.
- NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_assertion wasDerivedFrom befree-2016 NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_provenance.
- NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_assertion wasGeneratedBy ECO_0000203 NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_provenance.
- befree-2016 importedOn "2016-02-19" NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_provenance.