@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y> .
@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/v4.0.0/void/> .

dgn-np:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_head {
  this: np:hasAssertion dgn-np:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_assertion;
    np:hasProvenance dgn-np:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_provenance;
    np:hasPublicationInfo dgn-np:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_assertion a np:Assertion .
  
  dgn-np:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_provenance a np:Provenance .
  
  dgn-np:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_assertion {
  miriam-gene:8504 a ncit:C16612 .
  
  lld:C0282528 a ncit:C7057 .
  
  dgn-gda:DGN1aeeae63df64ce6b026ad4abdf61014a sio:SIO_000628 miriam-gene:8504, lld:C0282528;
    a sio:SIO_001121 .
}

dgn-np:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_provenance {
  dgn-np:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_assertion dcterms:description
      "[This case also raises a possibility that hydrops fetalis may be associated with a PEX3 gene defect and that peroxisomal disorders can be considered in the etiology of hydrops fetalis as well as other cell organelle disorders when one is considering yet undiscovered complementation groups in peroxisomal disorders.]. 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:20033294;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP783502.RAifeBmRrtaRodxxD5RiX08B1R4A89vLAPGs2MJS2RC7Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:40+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}