@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA> .
@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:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_head {
  this: np:hasAssertion dgn-np:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_assertion;
    np:hasProvenance dgn-np:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_provenance;
    np:hasPublicationInfo dgn-np:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_assertion a np:Assertion .
  
  dgn-np:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_provenance a np:Provenance .
  
  dgn-np:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_assertion {
  miriam-gene:2332 a ncit:C16612 .
  
  lld:C0011581 a ncit:C7057 .
  
  dgn-gda:DGN0fa5f08de5909770a26a5ab5d1680bb3 sio:SIO_000628 miriam-gene:2332, lld:C0011581;
    a sio:SIO_001121 .
}

dgn-np:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_provenance {
  dgn-np:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_assertion dcterms:description
      "[To learn more about this in a clinical setting, we asked 33 women with the FMR1 premutation and 20 women without the FMR1 premutation to complete the Brief Carroll Depression Scale (Brief CDS) and the Multidimensional Anxiety Questionnaire (MAQ) and to provide information about mental health medication use.]. 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:20629912;
    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:NP451829.RAfBgJvh4TGWTVWpgoOhbm9S12Gooc6EFAXej2ojtAtvA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:29+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" .
}