@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_head {
  this: np:hasAssertion dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_assertion;
    np:hasProvenance dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_provenance;
    np:hasPublicationInfo dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_assertion a np:Assertion .
  
  dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_provenance a np:Provenance .
  
  dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_assertion {
  miriam-gene:3064 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGNde0ff7f1d3e44b65d849c37bd202bce9 sio:SIO_000628 miriam-gene:3064, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_provenance {
  dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_assertion dcterms:description
      "[HIP14 is dysfunctional in the presence of mutant HTT (mHTT), the causative gene for Huntington disease (HD), and we hypothesize that reduced palmitoylation of HTT and other HIP14 substrates contributes to the pathogenesis of the disease.]. 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:24705354;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:00+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}