@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_head {
  this: np:hasAssertion dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_assertion ;
    np:hasProvenance dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_provenance ;
    np:hasPublicationInfo dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_assertion a np:Assertion .
  dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_provenance a np:Provenance .
  dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  lld:C0878544 a ncit:C7057 .
  dgn-gda:DGNbde657a37b24c1fc6b972cac9b83204c sio:SIO_000628 miriam-gene:1756 , lld:C0878544 ;
    a sio:SIO_001122 .
}
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_provenance {
  dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_assertion dcterms:description "[ Early diagnosis and treatment of DCM may lead to ventricular remodeling in DMD/BMD patients. Specific dystrophin gene mutations appear to be predictive of cardiac involvement, while other mutations may protect against or inhibit development of DCM. Further studies evaluating the impact of early intervention strategies on left ventricular geometry and function in muscular dystrophy patients seem warranted.]. 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:16246949 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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:disgenetrdf ;
    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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}