Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_provenance.
- NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_assertion wasGeneratedBy ECO_0000203 NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_provenance.
- NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_assertion wasDerivedFrom befree-20140225 NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_provenance.
- NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_assertion SIO_000772 11739371 NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_provenance.
- NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_assertion evidence source_evidence_literature NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_provenance.
- NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_assertion description "[Lafora disease (progressive myoclonus epilepsy of Lafora type) is an autosomal recessive neurodegenerative disorder resulting from defects in the EPM2A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP895020.RAMTJZ2t4VEvW-2r0x57ppQizLRzj1SKhNyQy9K2fKXGI130_provenance.