@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4> .
@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:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_head {
  this: np:hasAssertion dgn-np:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_assertion;
    np:hasProvenance dgn-np:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_provenance;
    np:hasPublicationInfo dgn-np:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_assertion a np:Assertion .
  
  dgn-np:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_provenance a np:Provenance .
  
  dgn-np:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_assertion {
  miriam-gene:28955 a ncit:C16612 .
  
  lld:C0004364 a ncit:C7057 .
  
  dgn-gda:DGN7ff78f42b5f8c8bc22ae10ce4231a45d sio:SIO_000628 miriam-gene:28955, lld:C0004364;
    a sio:SIO_001121 .
}

dgn-np:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_provenance {
  dgn-np:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_assertion dcterms:description
      "[Taken together, these data indicate that although the causal variants in the 16p13 region lie within CLEC16A, DEXI is an unappreciated autoimmune disease candidate gene, and illustrate the power of the 3C approach in progressing from genome-wide association studies results to candidate causal genes.]. 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:21989056;
    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:NP267306.RANdJ5NJQeQGjLsgyZySOdOIrYFXsWn6yWlXP14ti-ge4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:29+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" .
}