@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to> .
@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:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_head {
  this: np:hasAssertion dgn-np:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_assertion;
    np:hasProvenance dgn-np:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_provenance;
    np:hasPublicationInfo dgn-np:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_assertion a np:Assertion .
  
  dgn-np:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_provenance a np:Provenance .
  
  dgn-np:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_assertion {
  miriam-gene:5053 a ncit:C16612 .
  
  lld:C0031485 a ncit:C7057 .
  
  dgn-gda:DGNb99332a32c06ab9bca027c59bce7bab9 sio:SIO_000628 miriam-gene:5053, lld:C0031485;
    a sio:SIO_001121 .
}

dgn-np:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_provenance {
  dgn-np:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_assertion dcterms:description
      "[In order to determine the phenylketonuria (PKU) mutation spectrum in the population of Minas Gerais State, Brazil, 78 unrelated PKU patients found by the neonatal screening program from 1993 to 2003 were tested for nine phenylalanine hydroxylase mutations.]. 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:16755493;
    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:NP553263.RAc4u7AE3NWMObY1cOtF9N97XuXP5gTEeg4DlyStPC1to130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:55+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" .
}