Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_provenance.
- NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_assertion description "[Myotonic dystrophy types 1 (DM1) and 2 (DM2/proximal myotonic myopathy PROMM) are dominantly inherited disorders with unusual multisystemic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_provenance.
- NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_assertion evidence source_evidence_literature NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_provenance.
- NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_assertion SIO_000772 12601109 NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_provenance.
- NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_assertion wasDerivedFrom befree-20140225 NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_provenance.
- NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_assertion wasGeneratedBy ECO_0000203 NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_provenance.