Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_provenance.
- NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_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." NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_provenance.
- NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_assertion evidence source_evidence_literature NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_provenance.
- NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_assertion SIO_000772 8737929 NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_provenance.
- NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_assertion wasDerivedFrom befree-20140225 NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_provenance.
- NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_assertion wasGeneratedBy ECO_0000203 NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP166191.RAvIYyeoNMbA6Sbx8o52VqESbvj82n2H87o90YVHV1ORk130_provenance.