@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk> .
@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:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_head {
  this: np:hasAssertion dgn-np:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_assertion;
    np:hasProvenance dgn-np:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_provenance;
    np:hasPublicationInfo dgn-np:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_assertion a np:Assertion .
  
  dgn-np:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_provenance a np:Provenance .
  
  dgn-np:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_assertion {
  miriam-gene:1594 a ncit:C16612 .
  
  lld:C0206682 a ncit:C7057 .
  
  dgn-gda:DGNc241c1823820aaffe964d3f36eb261e4 sio:SIO_000628 miriam-gene:1594, lld:C0206682;
    a sio:SIO_001121 .
}

dgn-np:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_provenance {
  dgn-np:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_assertion dcterms:description
      "[Further, while the alleles AA and FF of the ApaI (rs7975232) and FokI (rs10735810) VDR polymorphisms and the haplotype tABF confer to protection from follicular carcinoma, the haplotype Tabf appeared to be associated with an increased FTC risk.]. 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:19499989;
    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:NP283229.RAVjdZA7FmXjfp5PHMjLxsEF0tS0HkMs5647TO0cqoowk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:39+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" .
}