@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY> .
@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/v4.0.0/void/> .

dgn-np:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_head {
  this: np:hasAssertion dgn-np:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_assertion;
    np:hasProvenance dgn-np:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_provenance;
    np:hasPublicationInfo dgn-np:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_assertion a np:Assertion .
  
  dgn-np:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_provenance a np:Provenance .
  
  dgn-np:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_assertion {
  miriam-gene:6571 a ncit:C16612 .
  
  lld:C0740858 a ncit:C7057 .
  
  dgn-gda:DGNdd69e0d20bd8ad3f809f020586eb7d2b sio:SIO_000628 miriam-gene:6571, lld:C0740858;
    a sio:SIO_001121 .
}

dgn-np:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_provenance {
  dgn-np:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_assertion dcterms:description
      "[Examination of VMAT2 variants can provide potential insights into roles for allelic variants at these loci in variant drug responses and in diseases linked to monoaminergic systems, including substance abuse and Parkinson's disease.]. 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:11099463;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP301804.RAwmHfORyG2TCZrVoSfKgVfb_DhC7J2J7tmlMd5FBiEkY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:02+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}