@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA> .
@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:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_head {
  this: np:hasAssertion dgn-np:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_assertion;
    np:hasProvenance dgn-np:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_provenance;
    np:hasPublicationInfo dgn-np:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_assertion a np:Assertion .
  
  dgn-np:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_provenance a np:Provenance .
  
  dgn-np:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_assertion {
  miriam-gene:10142 a ncit:C16612 .
  
  lld:C0007194 a ncit:C7057 .
  
  dgn-gda:DGN59dff8aa1d745a255354849dc4f5fe9a sio:SIO_000628 miriam-gene:10142, lld:C0007194;
    a sio:SIO_001121 .
}

dgn-np:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_provenance {
  dgn-np:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_assertion dcterms:description
      "[In addition to new mutations in known SCD genes, several novel genes not previously implicated in SCD causation have been found, particularly in long QT syndrome (e.g., KCNJ5, AKAP9, SNTA1), idiopathic ventricular fibrillation (e.g., DPP6, KCNJ8), dilated cardiomyopathy (e.g., NEBL), and hypertrophic cardiomyopathy (HCM; e.g., NEXN).]. 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:21430528;
    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:NP881813.RAYEoaT83Bn53UeJR_ZhaBVVFIrHnxoMBaqQRQJwV9ihA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:24+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" .
}