Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance.
- NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_assertion wasGeneratedBy ECO_0000203 NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance.
- NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_assertion wasDerivedFrom lhgdn-20090331 NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance.
- NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_assertion SIO_000772 15304595 NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance.
- NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_assertion evidence source_evidence_literature NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance.
- NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_assertion description "[a rare polymorphism at codon 171 (Asn-- > Ser) of human Prnp is associated with symptomatic epilepsies related to different forms of malformations of cortical development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206332.RATWPZyzu83Er4TYwOVwcF7bx_0sTBSNYnOEQx6vy-lCM130_provenance.