@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I> .
@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 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:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_head {
  this: np:hasAssertion dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_assertion ;
    np:hasProvenance dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_provenance ;
    np:hasPublicationInfo dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_assertion a np:Assertion .
  dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_provenance a np:Provenance .
  dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_assertion {
  miriam-gene:3356 a ncit:C16612 .
  lld:C1269683 a ncit:C7057 .
  dgn-gda:DGN87b9723c9ba8412cd715b5073f09cbef sio:SIO_000628 miriam-gene:3356 , lld:C1269683 ;
    a sio:SIO_001122 .
}
dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_provenance {
  dgn-np:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_assertion dct: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 ;
    sio:SIO_000772 miriam-pubmed:15052272 ;
    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:NP57298.RA5hJ7FRwfRZY0gX1Xzjk7LyDDdfR4ZQ0q8LWMA3Sxg1I130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}