@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak> .
@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/v3.0.0/void/> .

dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_head {
  this: np:hasAssertion dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_assertion;
    np:hasProvenance dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_provenance;
    np:hasPublicationInfo dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_assertion a np:Assertion .
  
  dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_provenance a np:Provenance .
  
  dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_assertion {
  miriam-gene:8929 a ncit:C16612 .
  
  lld:C3203358 a ncit:C7057 .
  
  dgn-gda:DGNab4c4bf0429abb8a8c494027413b3b43 sio:SIO_000628 miriam-gene:8929, lld:C3203358;
    a sio:SIO_001122 .
}

dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_provenance {
  dgn-np:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_assertion dcterms:description
      "[These results confirm a disturbance of cardiac autonomic regulation in CCHS, indicate that PHOX2B genotype is related to the severity of dysregulation, predict the need for cardiac pacemaker, and offer the clinician the potential to avert sudden death.]. 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:18041756;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP128182.RAdA058hyM8ahS9HCexPceUfRvRTiiI7tQTkN7ysH-cak130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:52+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}