Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance.
- NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_assertion description "[We also tested for the APP codon 693 mutation associated with hereditary cerebral hemorrhage with amyloidosis-Dutch type, for PRIP gene missense mutations at codons 102, 117, and 200, and for the PRIP insertion mutations which are associated with Creutzfeld-Jakob disease and Gerstmann-Straussler Scheinker syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance.
- NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_assertion evidence source_evidence_literature NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance.
- NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_assertion SIO_000772 1679288 NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance.
- NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_assertion wasDerivedFrom befree-20140225 NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance.
- NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_assertion wasGeneratedBy ECO_0000203 NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP825169.RAdFZ436arov8Cf9y6YWcWc6Ya1H4RyWvtVEDtWXFRW3M130_provenance.