@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o> .
@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:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_head {
  this: np:hasAssertion dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_assertion ;
    np:hasProvenance dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_provenance ;
    np:hasPublicationInfo dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_assertion a np:Assertion .
  dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_provenance a np:Provenance .
  dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_assertion {
  miriam-gene:3251 a ncit:C16612 .
  lld:C0000768 a ncit:C7057 .
  dgn-gda:DGN1def347b2c9740c47a189fc032baa916 sio:SIO_000628 miriam-gene:3251 , lld:C0000768 ;
    a sio:SIO_001121 .
}
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_provenance {
  dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_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:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
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}