@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA> .
@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:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_head {
  this: np:hasAssertion dgn-np:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_assertion;
    np:hasProvenance dgn-np:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_provenance;
    np:hasPublicationInfo dgn-np:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_assertion a np:Assertion .
  
  dgn-np:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_provenance a np:Provenance .
  
  dgn-np:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C1449563 a ncit:C7057 .
  
  dgn-gda:DGNdc0b9bfb70e4091bec0a8ba312d23e05 sio:SIO_000628 miriam-gene:1756, lld:C1449563;
    a sio:SIO_001121 .
}

dgn-np:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_provenance {
  dgn-np:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_assertion dcterms:description
      "[The etiology of familial risk was not evident in this pedigree before retrospective cardiovascular genetics assessment, highlighting ongoing diagnostic challenges and limitations of standardized screening panels (which do not include dystrophin) in patients with `idiopathic` DCM.]. 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:20206892;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP202634.RADVwIw1AEqI4ahljQ2eQx8gwUHuJxhjKvXAzfd64KSGA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:51+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" .
}