Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_provenance.
- NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_assertion description "[The most frequent transthyretin (TTR) variant associated with hereditary amyloidosis is TTR Met 30, which has its major focus in Portugal, although it also occurs in many other countries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_provenance.
- NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_assertion evidence source_evidence_literature NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_provenance.
- NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_assertion SIO_000772 7649556 NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_provenance.
- NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_assertion wasDerivedFrom befree-2016 NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_provenance.
- NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_assertion wasGeneratedBy ECO_0000203 NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_provenance.
- befree-2016 importedOn "2016-02-19" NP1316502.RAuGsHAvbbuCcuyJPVE-gnfC5WI7gLMeDinGPKFTLBZ94130_provenance.