@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_head {
  this: np:hasAssertion dgn-np:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_assertion;
    np:hasProvenance dgn-np:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance;
    np:hasPublicationInfo dgn-np:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_assertion a np:Assertion .
  
  dgn-np:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance a np:Provenance .
  
  dgn-np:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_assertion {
  miriam-gene:5226 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN4a43ba84a9fa7a292917b25b0156066b sio:SIO_000628 miriam-gene:5226, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_provenance {
  dgn-np:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_assertion dcterms:description
      "[Novel indications for PGD not readily applicable by traditional prenatal genetic diagnosis include avoiding clinical pregnancy termination, performing preconceptional diagnosis (polar body I), obtaining prenatal diagnosis without disclosure of prenatal genotype (nondisclosure), diagnosing adult-onset disorders particularly cancer, and identifying HLA compatible embryos suitable for recovering umbilical cord blood stem cells.]. 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:20572111;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP616916.RARPtrDfSLDU_RfopZAVScPkTTy3IYf-Mk5YZdR1il3p4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:49+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}