@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA> .
@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:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_head {
  this: np:hasAssertion dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_assertion;
    np:hasProvenance dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_provenance;
    np:hasPublicationInfo dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_assertion a np:Assertion .
  
  dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_provenance a np:Provenance .
  
  dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_assertion {
  miriam-gene:410 a ncit:C16612 .
  
  lld:C0268547 a ncit:C7057 .
  
  dgn-gda:DGNc14a03f2095c39114a19434bc6c808dc sio:SIO_000628 miriam-gene:410, lld:C0268547;
    a sio:SIO_001121 .
}

dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_provenance {
  dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_assertion dcterms:description
      "[It was concluded that the correction of ASA deficiency by a recombinant adenovirus that potentially could be used to transfer the gene to the brain, and gene therapy for MLD based on gene transfer of the ASA gene to mutant cells will be feasible because the overexpression of ASA in cells does not lead to profound deficiency of other sulfatases or result in a new phenotype.]. 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:8677802;
    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:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:02+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" .
}