@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8> .
@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:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_head {
  this: np:hasAssertion dgn-np:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_assertion;
    np:hasProvenance dgn-np:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_provenance;
    np:hasPublicationInfo dgn-np:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_assertion a np:Assertion .
  
  dgn-np:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_provenance a np:Provenance .
  
  dgn-np:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_assertion {
  miriam-gene:5226 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGN754fb6c9593d4f2d7e70bd22d65cf4a5 sio:SIO_000628 miriam-gene:5226, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_provenance {
  dgn-np:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_assertion dcterms:description
      "[PGD can be used to reduce the risk of transferring to the uterus an embryo with Down syndrome, and parents who are carriers of severe genetic diseases may choose to avoid having children with these debilitating genetic conditions.]. 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:18983739;
    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:NP505581.RAM8y8LuaPLf3Yv3_Uz52Pvo8OXL69WIrGytYmgyzj6v8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:01+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" .
}