@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4> .
@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:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_head {
  this: np:hasAssertion dgn-np:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_assertion;
    np:hasProvenance dgn-np:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_provenance;
    np:hasPublicationInfo dgn-np:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_assertion a np:Assertion .
  
  dgn-np:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_provenance a np:Provenance .
  
  dgn-np:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_assertion {
  miriam-gene:6530 a ncit:C16612 .
  
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dgn-np:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_provenance {
  dgn-np:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_assertion dcterms:description
      "[In this study, we examined the effect of the hA53T mutation during development by analyzing the protein expression of norepinephrine (NET), serotonin (SERT), and dopamine (DAT) transporters in addition to assessing locomotor and anxiety-like behavior.]. 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: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 .
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dgn-np:NP317748.RAZJO4bxin5QG50PKjbRIVekQHDMN4IpCJjwuFUqigfo4130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
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