@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw> .
@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:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_head {
  this: np:hasAssertion dgn-np:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_assertion;
    np:hasProvenance dgn-np:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_provenance;
    np:hasPublicationInfo dgn-np:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_assertion a np:Assertion .
  
  dgn-np:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_provenance a np:Provenance .
  
  dgn-np:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_assertion {
  miriam-gene:100379198 a ncit:C16612 .
  
  lld:C0812393 a ncit:C7057 .
  
  dgn-gda:DGN246425240915ef9449777eaf120e5a2c sio:SIO_000628 miriam-gene:100379198,
      lld:C0812393;
    a sio:SIO_001121 .
}

dgn-np:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_provenance {
  dgn-np:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_assertion dcterms:description
      "[The aim of the present study was to test for an association between two HTR2A polymorphisms (rs7997012 and rs6311), their interaction and the Montgomery and Åsberg Depression Rating Scale (MADRS) score change after ECT or SSRI treatment.]. 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:21741447;
    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:NP709261.RA_DhehRWyek5Mva4NhBqTVsawWvtBkUjmj2WDnloLAPw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:11+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}