@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM> .
@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:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_head {
  this: np:hasAssertion dgn-np:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_assertion ;
    np:hasProvenance dgn-np:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_provenance ;
    np:hasPublicationInfo dgn-np:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_assertion a np:Assertion .
  dgn-np:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_provenance a np:Provenance .
  dgn-np:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_assertion {
  miriam-gene:5226 a ncit:C16612 .
  lld:C0037176 a ncit:C7057 .
  dgn-gda:DGN10e32948f6302243c9b6026e15c0097b sio:SIO_000628 miriam-gene:5226 , lld:C0037176 ;
    a sio:SIO_001121 .
}
dgn-np:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_provenance {
  dgn-np:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_assertion dcterms:description "[Preimplantation genetic diagnosis (PGD) of single gene defects following assisted conception typically involves removal of single cells from preimplantation embryos and analysis using highly sensitive PCR amplification methods taking stringent precautions to prevent contamination from foreign or previously amplified DNA.]. 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:15322224 ;
    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:NP928990.RA712s3YkKUQplrf59RMdYboN4q1wEvlymZzK4_YHfMrM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:29+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" .
}