@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4> .
@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:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_head {
  this: np:hasAssertion dgn-np:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_assertion;
    np:hasProvenance dgn-np:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_provenance;
    np:hasPublicationInfo dgn-np:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_assertion a np:Assertion .
  
  dgn-np:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_provenance a np:Provenance .
  
  dgn-np:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_assertion {
  miriam-gene:2099 a ncit:C16612 .
  
  lld:C0005586 a ncit:C7057 .
  
  dgn-gda:DGN76f6c86320f0245069c3977c381dd53b sio:SIO_000628 miriam-gene:2099, lld:C0005586;
    a sio:SIO_001122 .
}

dgn-np:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_provenance {
  dgn-np:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_assertion dcterms:description
      "[The estrogen receptor alpha (ERalpha) gene in particular has been a subject of interest and has recently been intensively screened for variations of potential relevance to psychiatric disorders, resulting in the identification of four mutations in individuals with bipolar disorder or puerperal psychosis.]. 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:12627470;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP88250.RAkbSt2gcn0eCIYHQh26nIETSn_U7osPjqnzyjCBaTNO4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:43+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" .
}