@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo> .
@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:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_head {
  this: np:hasAssertion dgn-np:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_assertion;
    np:hasProvenance dgn-np:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_provenance;
    np:hasPublicationInfo dgn-np:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_assertion a np:Assertion .
  
  dgn-np:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_provenance a np:Provenance .
  
  dgn-np:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_assertion {
  miriam-gene:6584 a ncit:C16612 .
  
  lld:C0007194 a ncit:C7057 .
  
  dgn-gda:DGN78d339fc918552556c7ba67e25ef8dd6 sio:SIO_000628 miriam-gene:6584, lld:C0007194;
    a sio:SIO_001121 .
}

dgn-np:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_provenance {
  dgn-np:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_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:NP881816.RAb_jDcGzwzF7tGCkrH-mOo5LCpIfv9KclmVYXRgo9YBo130_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" .
}