sub:provenance {
  sub:assertion dcterms:description "[In the present study, the entire coding sequences and flanking regions of 12�major disease�(cardiomyopathy)-related genes [namely myosin, heavy chain�7, cardiac muscle,�?�(MYH7); myosin binding protein�C, cardiac�(MYBPC3); lamin A/C�(LMNA); troponin�I type�3�(cardiac)�(TNNI3); troponin�T type�2 (cardiac)�(TNNT2); actin,�?, cardiac muscle�1�(ACTC1); tropomyosin�1�(?)�(TPM1); sodium channel, voltage gated, type�V alpha subunit�(SCN5A); myosin, light chain�2, regulatory, cardiac, slow�(MYL2); myosin, heavy chain�6, cardiac muscle,�?�(MYH6); myosin, light chain�3, alkali, ventricular, skeletal, slow�(MYL3); and protein kinase, AMP-activated, gamma�2 non-catalytic subunit �(PRKAG2)] in 8�patients with dilated cardiomyopathy�(DCM) and in 8�patients with hypertrophic cardiomyopathy�(HCM) were amplified and then sequenced using the Ion Torrent Personal Genome Machine�(PGM) system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:27082122 ;
    prov:wasDerivedFrom dgn-void:BEFREE ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:BEFREE pav:importedOn "2017-02-19"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}