Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_assertion> ?p ?o ?g. }
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- NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_assertion type Assertion NP615494.RAcpL1qt4xW0S5_nfChf-fLzQz11rH1ViaVZdoAaCLdoU130_head.
- 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.