@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI> .
@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:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_head {
  this: np:hasAssertion dgn-np:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_assertion;
    np:hasProvenance dgn-np:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_provenance;
    np:hasPublicationInfo dgn-np:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_assertion a np:Assertion .
  
  dgn-np:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_provenance a np:Provenance .
  
  dgn-np:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_assertion {
  miriam-gene:2477 a ncit:C16612 .
  
  lld:C0154208 a ncit:C7057 .
  
  dgn-gda:DGN0d2d348c2eab504711cde97ff719a819 sio:SIO_000628 miriam-gene:2477, lld:C0154208;
    a sio:SIO_001121 .
}

dgn-np:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_provenance {
  dgn-np:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_assertion dcterms:description
      "[The association between FMR1 premutation and ovarian dysfunction has been widely studied, and many factors such as the repeat tract size, the sequence organization of the CGG repeat tract, the parental origin of the premutation, and the FMR1 mRNA levels have been examined.]. 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:19373114;
    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:NP894769.RA3SykwM2R34adLcGPDbCzSHuaIVFVRehglNodFUR0_aI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:10+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}