@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ> .
@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:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_head {
  this: np:hasAssertion dgn-np:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_assertion;
    np:hasProvenance dgn-np:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_provenance;
    np:hasPublicationInfo dgn-np:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_assertion a np:Assertion .
  
  dgn-np:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_provenance a np:Provenance .
  
  dgn-np:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_assertion {
  miriam-gene:4842 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN42ffcb93a379613f2c8f1d244f129180 sio:SIO_000628 miriam-gene:4842, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_provenance {
  dgn-np:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_assertion dcterms:description
      "[To determine if NOS gene polymorphism affects the 5' flanking region that is immediately upstream of the transcription start site lying between the TATA element and CAATT boxes in PD, and differs significantly between patients with PD and normal controls, we studied genetic polymorphism in that region of the neuronal NOS gene in Chinese patients with PD living in Taiwan.]. 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:11809160;
    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 .
}

dgn-np:NP599524.RAjXmuDoTM9RuDOSqSf3IT0CbO35vsXzSt9q7-FZD7RfQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:00+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" .
}