@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98> .
@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:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_head {
  this: np:hasAssertion dgn-np:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_assertion;
    np:hasProvenance dgn-np:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_provenance;
    np:hasPublicationInfo dgn-np:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_assertion a np:Assertion .
  
  dgn-np:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_provenance a np:Provenance .
  
  dgn-np:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_assertion {
  miriam-gene:1621 a ncit:C16612 .
  
  lld:C0152116 a ncit:C7057 .
  
  dgn-gda:DGN456dfe5ca4bd7781de87b5252fba61d1 sio:SIO_000628 miriam-gene:1621, lld:C0152116;
    a sio:SIO_001121 .
}

dgn-np:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_provenance {
  dgn-np:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_assertion dcterms:description
      "[The genetic study of plasma DBH activity allowed to discriminate between two forms of spasmodic torticollis, one, which is most likely linked to familial torsion dystonia, appears to be associated with altered dopaminergic activity, while the other, nonfamilial with normal sympathetic activity, is probably an idiopathic or sporadic form of spasmodic torticollis.]. 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:7312142;
    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:NP592738.RAFdbRTX88etbB-QgEwXXQWQAPikVFVeJSgFhx5o2lk98130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:56+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: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" .
}