Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_provenance.
- NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_assertion description "[CNS involvement is rare in systemic amyloidoses due to transthyretin (TTR) mutation and manifests as a combination of dementia, seizures, and myelopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_provenance.
- NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_assertion evidence source_evidence_literature NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_provenance.
- NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_assertion SIO_000772 11445644 NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_provenance.
- NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_assertion wasDerivedFrom befree-2016 NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_provenance.
- NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_assertion wasGeneratedBy ECO_0000203 NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_provenance.
- befree-2016 importedOn "2016-02-19" NP323385.RAYXJZ6lU65lUcR8GWWDLPX2n9h1bnjU0i0f4tAD4pm_A130_provenance.