@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE> .
@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:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_head {
  this: np:hasAssertion dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_assertion ;
    np:hasProvenance dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_provenance ;
    np:hasPublicationInfo dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_assertion a np:Assertion .
  dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_provenance a np:Provenance .
  dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_assertion {
  miriam-gene:5226 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN5f3a9ce3899b8c4b559449f2e8599e22 sio:SIO_000628 miriam-gene:5226 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_provenance {
  dgn-np:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_assertion dcterms:description "[Despite the numerous ethical objections and legal arguments, PGD for adult-onset cancers is today a reality and couples with an inherited predisposing mutation deserve the same respect, support and right to choose if their child will be born having an extremely high risk for cancer development as in the case of other life-threatening diseases for which prenatal screening has become a standard.]. 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:19785065 ;
    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:NP534614.RAeuoo6hx_lvzk6XUWWbjyQg98tYTKRYrVD88LNEl9tLE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:22+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> ;
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}