@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8> .
@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:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_head {
  this: np:hasAssertion dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_assertion;
    np:hasProvenance dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_provenance;
    np:hasPublicationInfo dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_assertion a np:Assertion .
  
  dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_provenance a np:Provenance .
  
  dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_assertion {
  miriam-gene:5428 a ncit:C16612 .
  
  lld:C0025322 a ncit:C7057 .
  
  dgn-gda:DGN7266fd920e4af6701b9858000df6ad8f sio:SIO_000628 miriam-gene:5428, lld:C0025322;
    a sio:SIO_001121 .
}

dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_provenance {
  dgn-np:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_assertion dcterms:description
      "[The study objective was to determine if mutations in mitochondrial DNA polymerase gamma (POLG) are associated with spontaneous 46,XX primary ovarian insufficiency (sPOI) using restriction fragment length polymorphism analysis of genomic DNA.]. 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:20701905;
    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:NP372508.RALHK7ytOlo_-iageato29pJJOFl8Z92P33WiOU8a5Au8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+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" .
}