Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance.
- NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_assertion description "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance.
- NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_assertion evidence source_evidence_literature NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance.
- NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_assertion SIO_000772 23797140 NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance.
- NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_assertion wasDerivedFrom befree-20140225 NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance.
- NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_assertion wasGeneratedBy ECO_0000203 NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance.
- befree-20140225 importedOn "2014-02-25" NP788375.RAfRB6hOdvK3fXI1SCI1XqgajH5H6OBYi_jAJd6THM8po130_provenance.