Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_provenance.
- NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_assertion description "[Familial amyloidotic polyneuropathy type IV, or Gelsolin amyloidosis (GA), is a rare condition caused by G654A or G654T mutation in gelsolin gene at 9q32-34.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_provenance.
- NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_assertion evidence source_evidence_literature NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_provenance.
- NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_assertion SIO_000772 22512621 NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_provenance.
- NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_assertion wasDerivedFrom befree-20140225 NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_provenance.
- NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_assertion wasGeneratedBy ECO_0000203 NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP452478.RAs9rhG6Q-TeiMkoeraveMb4y4YD8xTT-5fOekgc43T3Q130_provenance.