@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE> .
@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:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_head {
  this: np:hasAssertion dgn-np:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_assertion;
    np:hasProvenance dgn-np:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_provenance;
    np:hasPublicationInfo dgn-np:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_assertion a np:Assertion .
  
  dgn-np:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_provenance a np:Provenance .
  
  dgn-np:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_assertion {
  miriam-gene:3251 a ncit:C16612 .
  
  lld:C0025521 a ncit:C7057 .
  
  dgn-gda:DGN8d1e24fe82adba0c1afa8457e6ffccab sio:SIO_000628 miriam-gene:3251, lld:C0025521;
    a sio:SIO_001121 .
}

dgn-np:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_provenance {
  dgn-np:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_assertion dcterms:description
      "[Further work with these and other vector constructions is underway in the hope that this technique may allow safe and effective treatment of ADA and HPRT deficiencies, paving the way for treatments of other inborn errors of metabolism through somatic gene replacement therapy.]. 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:3555977;
    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:NP689476.RAPCtg3LpPDzPLSsbTkHkQ7SJwtG0WNjMheCEJ5zdi8sE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:59+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}