@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU> .
@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:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_head {
  this: np:hasAssertion dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_assertion;
    np:hasProvenance dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_provenance;
    np:hasPublicationInfo dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_assertion a np:Assertion .
  
  dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_provenance a np:Provenance .
  
  dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_assertion {
  miriam-gene:84627 a ncit:C16612 .
  
  lld:C0266539 a ncit:C7057 .
  
  dgn-gda:DGN38e95f8e0420235b7b7fb52c908df2df sio:SIO_000628 miriam-gene:84627, lld:C0266539;
    a sio:SIO_001121 .
}

dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_provenance {
  dgn-np:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_assertion dcterms:description
      "[Our findings suggest that in addition to rare variants in ZNF469 underlying CCT variation in BCS patients, more common variants near this gene may contribute to CCT variation in the general population.]. 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:20485516;
    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:NP381588.RAYbJviI3CjoVLK3nEC1zF-lpRxb2Y30gD25f_zhkIDvU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:45+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" .
}