Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_provenance.
- NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_assertion description "[Our study confirms that the PROMM phenotype is associated with DM2-(CCTG)(n) expansion mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_provenance.
- NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_assertion evidence source_evidence_literature NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_provenance.
- NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_assertion SIO_000772 15261229 NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_provenance.
- NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_assertion wasDerivedFrom befree-20140225 NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_provenance.
- NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_assertion wasGeneratedBy ECO_0000203 NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP181995.RAIxSNKrEPCswKeyWl8g4lr08THqTKzhRb4JifrqPs3Fc130_provenance.