Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_provenance.
- NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_assertion description "[A PrP cerebral amyloid angiopathy has not been reported in diseases caused by PRNP mutations or in human transmissible spongiform encephalopathies; we propose to name this phenotype PrP cerebral amyloid angiopathy (PrP-CAA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_provenance.
- NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_assertion evidence source_evidence_literature NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_provenance.
- NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_assertion SIO_000772 8570627 NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_provenance.
- NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_assertion wasDerivedFrom befree-20140225 NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_provenance.
- NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_assertion wasGeneratedBy ECO_0000203 NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP805610.RAbewxtI5mTN_6nn_MxMcDrfimu3Zja86b_HT3U1FXlrM130_provenance.