Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_provenance.
- NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_assertion description "[GSS may be more common than is currently realised; PrP gene analysis is potentially useful for diagnosis and genetic counselling in familial dementias and ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_provenance.
- NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_assertion evidence source_evidence_literature NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_provenance.
- NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_assertion SIO_000772 2567794 NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_provenance.
- NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_assertion wasDerivedFrom befree-20140225 NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_provenance.
- NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_assertion wasGeneratedBy ECO_0000203 NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP914214.RAk4116o3PZc5Y10TTSBVecXBF4Cny3vsSoSdxSgAtKcE130_provenance.