@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_head {
  this: np:hasAssertion dgn-np:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_assertion ;
    np:hasProvenance dgn-np:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_provenance ;
    np:hasPublicationInfo dgn-np:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_assertion a np:Assertion .
  dgn-np:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_provenance a np:Provenance .
  dgn-np:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_assertion {
  miriam-gene:3356 a ncit:C16612 .
  lld:C0752294 a ncit:C7057 .
  dgn-gda:DGNcc11e71aede29e6f0dc02ef23629295f sio:SIO_000628 miriam-gene:3356 , lld:C0752294 ;
    a sio:SIO_001122 .
}
dgn-np:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_provenance {
  dgn-np:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_assertion dcterms:description "[This is the first study that shows the association between 5HTR2A gene polymorphisms and polysymptomatic NE. These results provide further evidence suggesting that genetic variations at 5HTR2A may influence NE treatment response.]. 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:21089166 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP136259.RAcmzsaIcQdJvRitgA7kzGfetH2vTKiavXAP3HTxK2iv8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:56+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}