@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE> .
@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:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_head {
  this: np:hasAssertion dgn-np:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_assertion;
    np:hasProvenance dgn-np:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_provenance;
    np:hasPublicationInfo dgn-np:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_assertion a np:Assertion .
  
  dgn-np:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_provenance a np:Provenance .
  
  dgn-np:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_assertion {
  miriam-gene:784 a ncit:C16612 .
  
  lld:C0023976 a ncit:C7057 .
  
  dgn-gda:DGNd118d407e41b0255ffef5632010a6fe3 sio:SIO_000628 miriam-gene:784, lld:C0023976;
    a sio:SIO_001121 .
}

dgn-np:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_provenance {
  dgn-np:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_assertion dcterms:description
      "[The determination of the structures of the human CACNL1A2 and CACNLB3 genes should facilitate study of the role of these genes in the development of NIDDM and also other genetic diseases such as long QT syndrome.]. 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:7557998;
    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:NP502865.RAi0FVM9vLHxX9nJnJTc2aaFrX6so5EKxsGEylUdeazAE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:59+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" .
}