@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA> .
@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:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_head {
  this: np:hasAssertion dgn-np:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_assertion;
    np:hasProvenance dgn-np:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_provenance;
    np:hasPublicationInfo dgn-np:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_assertion a np:Assertion .
  
  dgn-np:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_provenance a np:Provenance .
  
  dgn-np:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_assertion {
  miriam-gene:3356 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
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dgn-np:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_provenance {
  dgn-np:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_assertion dcterms:description
      "[Our results suggested that genetic polymorphism of 102 T/C in the 5-HT2AR gene may have influence on the response to fluvoxamine treatment for patients with an autistic disorder. Because of the small numbers of subject studied here, further studies are needed. The methods of fluvoxamine treatment, such as appropriate dosage and treatment duration, should also be clarified.]. 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:NP57370.RAM_lVbDfgTxlSSow0zSNPrrnN-yhwpS8a7JO--I5HCQA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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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