@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk> .
@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:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_head {
  this: np:hasAssertion dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_assertion;
    np:hasProvenance dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_provenance;
    np:hasPublicationInfo dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_assertion a np:Assertion .
  
  dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_provenance a np:Provenance .
  
  dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_assertion {
  miriam-gene:1437 a ncit:C16612 .
  
  lld:C0026650 a ncit:C7057 .
  
  dgn-gda:DGN58047f8311d97ddded578d4b09c34caa sio:SIO_000628 miriam-gene:1437, lld:C0026650;
    a sio:SIO_001121 .
}

dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_provenance {
  dgn-np:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_assertion dcterms:description
      "[Rapid-onset dystonia-parkinsonism (RDP) is a genetic movement disorder characterized by abrupt onset over hours to days of bradykinesia, postural instability, dysphagia, dysarthria, and severe dystonic spasms with decreased levels of the dopamine metabolite, homovanillic acid (HVA), in cerebrospinal fluid (CSF).]. 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:9918356;
    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:NP897254.RATmCk6Jq1KpRACimYjwNLTEpfLABBHnlKJUaiKYVtxQk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:11+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" .
}