Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance.
- NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_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." NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance.
- NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_assertion evidence source_evidence_literature NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance.
- NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_assertion SIO_000772 8737929 NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance.
- NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_assertion wasDerivedFrom befree-20150227 NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance.
- NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_assertion wasGeneratedBy ECO_0000203 NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance.