Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_provenance.
- NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_assertion wasGeneratedBy ECO_0000203 NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_provenance.
- NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_assertion wasDerivedFrom befree-20150227 NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_provenance.
- NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_assertion SIO_000772 10781099 NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_provenance.
- NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_assertion evidence source_evidence_literature NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_provenance.
- NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_assertion description "[N-terminal sequence analysis of isolated leptomeningeal amyloid fibrils revealed homology to ABri, the peptide originated by a point mutation at the stop codon of gene BRI in familial British dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823889.RAXWvip2bfv0PMZxfrdeoNds42TCKEXhTQ57wkZ-o2YCA130_provenance.