@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU> .
@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/v4.0.0/void/> .

dgn-np:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_head {
  this: np:hasAssertion dgn-np:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_assertion;
    np:hasProvenance dgn-np:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_provenance;
    np:hasPublicationInfo dgn-np:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_assertion a np:Assertion .
  
  dgn-np:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_provenance a np:Provenance .
  
  dgn-np:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C3469521 a ncit:C7057 .
  
  dgn-gda:DGN29fce06ee8b5e3c5fc153a56435cf161 sio:SIO_000628 miriam-gene:675, lld:C3469521;
    a sio:SIO_001121 .
}

dgn-np:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_provenance {
  dgn-np:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_assertion dcterms:description
      "[In conclusion, we established the downstream FA genes FANCD2 and BRCA2 to represent particularly vulnerable parts of the FA pathway, providing direct evidence for the paradoxical assumption that their inactivation could be predominantly selected against in cancer 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:17387268;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP600988.RAlqNcOW2fPYP6hdBVlwrPEn4b3P1n0ubTTYVqnouvHfU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:18+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}