@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I> .
@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:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_head {
  this: np:hasAssertion dgn-np:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_assertion;
    np:hasProvenance dgn-np:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_provenance;
    np:hasPublicationInfo dgn-np:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_assertion a np:Assertion .
  
  dgn-np:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_provenance a np:Provenance .
  
  dgn-np:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_assertion {
  miriam-gene:2463 a ncit:C16612 .
  
  lld:C0015625 a ncit:C7057 .
  
  dgn-gda:DGN86b8a9137c9dc7fd8e9f652c7206d204 sio:SIO_000628 miriam-gene:2463, lld:C0015625;
    a sio:SIO_001121 .
}

dgn-np:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_provenance {
  dgn-np:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_assertion dcterms:description
      "[Both the total number of chromosome gaps and breaks and breaks at the specific common fragile sites FRA3B and FRA16D were significantly elevated in the absence of an intact FA pathway.]. 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:15661754;
    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:NP477155.RA2lWVK8ePdWYHDYrqG1RC_gi5SnfzUuIDk64mJQp8C2I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:21+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: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" .
}