Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion wasGeneratedBy ECO_0000203 NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion wasDerivedFrom befree-20150227 NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion SIO_000772 9354764 NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_assertion evidence source_evidence_literature NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.
- NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_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." NP436885.RA073voAQ_CviO_o_2ViWtnmu-7jJLK5xmv__1yisqyOU130_provenance.