@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo> .
@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:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_head {
  this: np:hasAssertion dgn-np:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_assertion;
    np:hasProvenance dgn-np:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_provenance;
    np:hasPublicationInfo dgn-np:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_assertion a np:Assertion .
  
  dgn-np:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_provenance a np:Provenance .
  
  dgn-np:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_assertion {
  miriam-gene:64979 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN44ca9aac5eb22435e939ee128c49c32a sio:SIO_000628 miriam-gene:64979, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_provenance {
  dgn-np:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_assertion dcterms:description
      "[Deleterious mutations in few genes involved in the Fanconi complex are responsible for Fanconi anemia at the homozygous state and breast cancer (BC) susceptibility at the heterozygous state (BRCA2, PALB2, BRIP1).]. 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:22725699;
    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:NP992343.RAFl0bIK6mCJQrhtM9OKE53TALa_rsnH-O1sK1Vat3Cfo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:15+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" .
}