@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8> .
@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:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_head {
  this: np:hasAssertion dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_assertion;
    np:hasProvenance dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_provenance;
    np:hasPublicationInfo dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_assertion a np:Assertion .
  
  dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_provenance a np:Provenance .
  
  dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  
  lld:C0020256 a ncit:C7057 .
  
  dgn-gda:DGN5cf97f130688d312c1c02698ecb667f1 sio:SIO_000628 miriam-gene:3918, lld:C0020256;
    a sio:SIO_001121 .
}

dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_provenance {
  dgn-np:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_assertion dcterms:description
      "[Here we show that conditional inactivation of the Hdh gene in Wnt1 cell lineages results in congenital hydrocephalus, implicating huntingtin for the first time in the regulation of cerebral spinal fluid (CSF) homeostasis.]. 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:18838463;
    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:NP387931.RAnpDEhfSWYNimypQe2O3kCyVfrzC3KLlqyhheWSCQ_Q8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:51+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" .
}