@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk> .
@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:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_head {
  this: np:hasAssertion dgn-np:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_assertion;
    np:hasProvenance dgn-np:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_provenance;
    np:hasPublicationInfo dgn-np:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_assertion a np:Assertion .
  
  dgn-np:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_provenance a np:Provenance .
  
  dgn-np:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_assertion {
  miriam-gene:9219 a ncit:C16612 .
  
  lld:C0398686 a ncit:C7057 .
  
  dgn-gda:DGN7c1f5c76b0a2acc30071a8eac0d8acb8 sio:SIO_000628 miriam-gene:9219, lld:C0398686;
    a sio:SIO_001121 .
}

dgn-np:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_provenance {
  dgn-np:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_assertion dcterms:description
      "[Among them, hereditary diseases such as the primary immunodeficiency diseases (PID) were considered suitable candidates for gene therapy because the therapeutic strategy was very simple, therefore, effective gene therapy may be obtained without significant difficulty compared to other more complex diseases such as cancer.]. 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:16472146;
    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:NP404691.RA4iVwcpnGbr1kNQuMMTI7Pfjufi2zFR4qluDAog7BdQk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:01+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" .
}