Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_provenance.
- NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_assertion wasGeneratedBy ECO_0000203 NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_provenance.
- NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_assertion wasDerivedFrom befree-20140225 NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_provenance.
- NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_assertion SIO_000772 9354764 NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_provenance.
- NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_assertion evidence source_evidence_literature NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_provenance.
- NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_assertion description "[Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant type of systemic amyloidosis caused by a G654A (Asn-187) or G654T (Tyr-187) mutation in the gelsolin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP552385.RAsG6yFaP8DDVrGWeRgKQgSK3CeUEXWce05blMjwkkrB0130_provenance.