@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI> .
@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:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_head {
  this: np:hasAssertion dgn-np:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_assertion;
    np:hasProvenance dgn-np:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_provenance;
    np:hasPublicationInfo dgn-np:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_assertion a np:Assertion .
  
  dgn-np:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_provenance a np:Provenance .
  
  dgn-np:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_assertion {
  miriam-gene:776 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGNac0cb7fc0a502c3fdc434d1af8def267 sio:SIO_000628 miriam-gene:776, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_provenance {
  dgn-np:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_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-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP277373.RAr3j78o8bM1pFiKirfjbiYD3bq-FaybLZLzxEgqQvPEI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:18+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" .
}