@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc> .
@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:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_head {
  this: np:hasAssertion dgn-np:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_assertion;
    np:hasProvenance dgn-np:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_provenance;
    np:hasPublicationInfo dgn-np:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_assertion a np:Assertion .
  
  dgn-np:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_provenance a np:Provenance .
  
  dgn-np:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_assertion {
  miriam-gene:3358 a ncit:C16612 .
  
  lld:C1269683 a ncit:C7057 .
  
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dgn-np:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_provenance {
  dgn-np:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_assertion dcterms:description
      "[Although these data should be interpreted cautiously due to the small sample size, these results implicate TPH1 and SLC6A4 in general response, and HTR2A, TPH2, and MAOA in the specificity of response to fluoxetine. Intriguingly, we observe that a number of the less frequent alleles of many of the SNP markers were associated with the nonresponse and nonspecific phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP57243.RArrNK-Z7KKwZbjJLjDUVmaIK62JXf7aTLrB6MxVKFZyc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
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