@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw> .
@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:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_head {
  this: np:hasAssertion dgn-np:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_assertion;
    np:hasProvenance dgn-np:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_provenance;
    np:hasPublicationInfo dgn-np:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_assertion a np:Assertion .
  
  dgn-np:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_provenance a np:Provenance .
  
  dgn-np:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_assertion {
  miriam-gene:1621 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGNc9f94d9a38d7d6970b5c9ca58959557b sio:SIO_000628 miriam-gene:1621, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_provenance {
  dgn-np:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_assertion dcterms:description
      "[Observed association of DBH SNP/SNP haplotypes with PD susceptibility and its role in modulating disease severity reiterates the importance of dopamine pathway in sporadic PD etiology in general and potential therapeutic implications of DBH in particular.]. 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:20498626;
    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:NP60177.RAVx20dSlaSpG40AV-wwNpqNAnqTx0vIoXu6n2P1ZPcGw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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>,
      <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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}