Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance.
- NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_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." NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance.
- NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_assertion evidence source_evidence_literature NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance.
- NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_assertion SIO_000772 23797140 NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance.
- NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_assertion wasDerivedFrom befree-20140225 NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance.
- NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_assertion wasGeneratedBy ECO_0000203 NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP776093.RA2S_QmYbbzYTXpyMdKlZWHs80fzS0B1hq-U5MXF9bpwY130_provenance.