@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0> .
@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:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_head {
  this: np:hasAssertion dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_assertion;
    np:hasProvenance dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_provenance;
    np:hasPublicationInfo dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_assertion a np:Assertion .
  
  dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_provenance a np:Provenance .
  
  dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_assertion {
  miriam-gene:23626 a ncit:C16612 .
  
  lld:C0085215 a ncit:C7057 .
  
  dgn-gda:DGNb0a61e372e7ca280793e46534737bb99 sio:SIO_000628 miriam-gene:23626, lld:C0085215;
    a sio:SIO_001122 .
}

dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_provenance {
  dgn-np:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_assertion dcterms:description
      "[The goal of this study was to determine whether mutations of meiotic genes, such as disrupted meiotic cDNA (DMC1), MutS homolog (MSH4), MSH5, and S. cerevisiae homolog (SPO11), were associated with premature ovarian failure (POF).]. 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:18166824;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP93008.RAeGPYCBlR5packRJNl2EJhuV2Lon9jc0F5o1CC7cD7N0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:46+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" .
}