@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_head {
  this: np:hasAssertion dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_assertion ;
    np:hasProvenance dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance ;
    np:hasPublicationInfo dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_assertion a np:Assertion .
  dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance a np:Provenance .
  dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_assertion {
  miriam-gene:4607 a ncit:C16612 .
  lld:C0007193 a ncit:C7057 .
  dgn-gda:DGN21b7504f592ffaaac5bb8fdf7663a25a sio:SIO_000628 miriam-gene:4607 , lld:C0007193 ;
    a sio:SIO_001121 .
}
dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance {
  dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_assertion dcterms:description "[Although cases of adult patients with DCM caused by mutations of the genes encoding sarcomeric or cytoskeletal proteins of cardiomyocytes are infrequent in Japan, it may be advisable to screen older DCM patients for MYBPC3 mutations, and male patients with familial DCM for dystrophin mutations.]. 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:15671604 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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 .
}
dgn-np:NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:21+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}