@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8> .
@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:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_head {
  this: np:hasAssertion dgn-np:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_assertion;
    np:hasProvenance dgn-np:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_provenance;
    np:hasPublicationInfo dgn-np:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_assertion a np:Assertion .
  
  dgn-np:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_provenance a np:Provenance .
  
  dgn-np:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_assertion {
  miriam-gene:2175 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGN63a85a30aa098e297cb713858a5f37b8 sio:SIO_000628 miriam-gene:2175, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_provenance {
  dgn-np:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_assertion dcterms:description
      "[We conclude that perturbations of as yet unidentified factors that govern the binding activity or intracellular localization of FANCA may promote cytogenetic instability and clonal progression in patients with AML who do not have Fanconi anemia.]. 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:12637330;
    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:NP193911.RAxMe6YLseqYlGRQ2Slg-D9Q8dgWGpJf85D1bl1X9qhG8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:46+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" .
}