@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM> .
@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:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_head {
  this: np:hasAssertion dgn-np:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_assertion;
    np:hasProvenance dgn-np:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_provenance;
    np:hasPublicationInfo dgn-np:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_assertion a np:Assertion .
  
  dgn-np:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_provenance a np:Provenance .
  
  dgn-np:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_assertion {
  miriam-gene:5663 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGN45aef0cce2eb427dfb78f79dbfd8c441 sio:SIO_000628 miriam-gene:5663, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_provenance {
  dgn-np:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_assertion dcterms:description
      "[These demonstrations of dysregulated Wnt signaling and presenilin-1 expression together with impaired expression of dopaminergic transcription factors reveal broad pleitropic neuro-regulatory defects played by HPRT expression and suggest new directions for investigating mechanisms of aberrant neurogenesis and neuropathology in LND and potential new targets for restoration of effective signaling in this neuro-developmental defect.]. 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:21305049;
    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:NP599682.RAXxfGTYJTscmd4F_bmYAAVt8kywwcrEzk7_tscKrA2PM130_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" .
}