Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_provenance.
- NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_assertion description "[The polymorphism in the human prion protein gene at codon 129 (PRNP 129) determines susceptibility to prion disease, and has been associated with early onset and a more severe course of other neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_provenance.
- NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_assertion evidence source_evidence_literature NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_provenance.
- NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_assertion SIO_000772 16543824 NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_provenance.
- NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_assertion wasDerivedFrom befree-2016 NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_provenance.
- NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_assertion wasGeneratedBy ECO_0000203 NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_provenance.
- befree-2016 importedOn "2016-02-19" NP540791.RAf2f27qePjH6DVgUmZ2XNu-P0VrKLEyamzK3w38EJTu0130_provenance.