@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw> .
@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:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_head {
  this: np:hasAssertion dgn-np:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_assertion;
    np:hasProvenance dgn-np:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_provenance;
    np:hasPublicationInfo dgn-np:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_assertion a np:Assertion .
  
  dgn-np:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_provenance a np:Provenance .
  
  dgn-np:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_assertion {
  miriam-gene:2177 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGN5fbbe7bd1f895a889fd612e61e166d80 sio:SIO_000628 miriam-gene:2177, lld:C0000768;
    a sio:SIO_001123 .
}

dgn-np:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_provenance {
  dgn-np:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_assertion dcterms:description
      "[Fancd2 is essential during embryogenesis to prevent inappropriate apoptosis in neural cells and other tissues undergoing high levels of proliferative expansion, implicating this mechanism in the congenital abnormalities observed in human infants with FA.]. 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:14667412;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP152916.RAlj1rPz7j0vHoZT0LnAzB2YuuF0RRwg68pcRUgTu1jYw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:21+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" .
}