@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8> .
@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:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_head {
  this: np:hasAssertion dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_assertion;
    np:hasProvenance dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_provenance;
    np:hasPublicationInfo dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_assertion a np:Assertion .
  
  dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_provenance a np:Provenance .
  
  dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  
  lld:C0018213 a ncit:C7057 .
  
  dgn-gda:DGN1db687bf9bbb2c7fba2cca39342a7107 sio:SIO_000628 miriam-gene:7421, lld:C0018213;
    a sio:SIO_001121 .
}

dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_provenance {
  dgn-np:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_assertion dcterms:description
      "[This is the largest and most comprehensive study of the VDR gene in GD to date and these data suggest that these polymorphisms of the VDR gene do not contribute to GD susceptibility in the UK.]. 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:15104566;
    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:NP613260.RASQwYIRFdu5b2e-vf8yy8YwEjarXhNb0qohk7RijyQe8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:10+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" .
}