Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_provenance.
- NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_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." NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_provenance.
- NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_assertion evidence source_evidence_literature NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_provenance.
- NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_assertion SIO_000772 11445644 NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_provenance.
- NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_assertion wasDerivedFrom befree-20150227 NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_provenance.
- NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_assertion wasGeneratedBy ECO_0000203 NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP761689.RALVO26ogti4_kGAfGXJNiAFt7hl3wGbvPdwK2-lE8PTw130_provenance.