@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E> .
@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:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_head {
  this: np:hasAssertion dgn-np:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_assertion;
    np:hasProvenance dgn-np:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_provenance;
    np:hasPublicationInfo dgn-np:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_assertion a np:Assertion .
  
  dgn-np:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_provenance a np:Provenance .
  
  dgn-np:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_assertion {
  miriam-gene:181 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGNa3c5c5bf2d1db537762dc44da70c8250 sio:SIO_000628 miriam-gene:181, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_provenance {
  dgn-np:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_assertion dcterms:description
      "[We argue that both normal and abnormal development in children conceived by ART can be explained by epigenetic mechanisms, which control the establishment and maintenance of gene expression patterns in the placenta and fetus.]. 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:15994847;
    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:NP628643.RAq6P2GED2isgWK_eurE513JT_nfaYZRLgacQWL5RQB2E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:19+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" .
}