Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_provenance.
- NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_assertion description "[This conversion is important for PrP amyloidogenesis, which occurs to the highest degree in the genetically determined Gerstmann-Str�ussler-Scheinker disease (GSS) and prion protein cerebral amyloid angiopathy (PrP-CAA), while it is less frequently seen in other prion diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_provenance.
- NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_assertion evidence source_evidence_literature NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_provenance.
- NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_assertion SIO_000772 8737929 NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_provenance.
- NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_assertion wasDerivedFrom befree-2016 NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_provenance.
- NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_assertion wasGeneratedBy ECO_0000203 NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP1354708.RAlZ4vRFsawKstpIpeZW_MLeREhwTPDbkQsYg37GbcK1Q130_provenance.