@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM> .
@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:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_head {
  this: np:hasAssertion dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_assertion;
    np:hasProvenance dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_provenance;
    np:hasPublicationInfo dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_assertion a np:Assertion .
  
  dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_provenance a np:Provenance .
  
  dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_assertion {
  miriam-gene:4942 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGN6a4bed26073346de19062e62d875eaf4 sio:SIO_000628 miriam-gene:4942, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_provenance {
  dgn-np:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_assertion dcterms:description
      "[With the final goal of applying gene therapy to this human genetic disease, we have established an in vitro model to test the correction of OAT enzymatic deficiency in mammalian cells, using OAT recombinant retroviruses.]. 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:7712330;
    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:NP917389.RAX9YXFvSO8uxwWqWiQMsjl0bjoKR_WqqkDVDQ3PUb4xM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:23+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" .
}