Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance.
- NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_assertion wasGeneratedBy ECO_0000203 NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance.
- NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_assertion wasDerivedFrom befree-20140225 NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance.
- NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_assertion SIO_000772 22407275 NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance.
- NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_assertion evidence source_evidence_literature NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance.
- NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP461057.RAeMX9sZhOlBamhQtqdbeRvb7mRoA3S_RqsIRPz3_xoEc130_provenance.