@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU> .
@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:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_head {
  this: np:hasAssertion dgn-np:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_assertion;
    np:hasProvenance dgn-np:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_provenance;
    np:hasPublicationInfo dgn-np:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_assertion a np:Assertion .
  
  dgn-np:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_provenance a np:Provenance .
  
  dgn-np:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_assertion {
  miriam-gene:79874 a ncit:C16612 .
  
  lld:C1458155 a ncit:C7057 .
  
  dgn-gda:DGNa10308c6fc905b01868d85945c1f1817 sio:SIO_000628 miriam-gene:79874, lld:C1458155;
    a sio:SIO_001121 .
}

dgn-np:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_provenance {
  dgn-np:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_assertion dcterms:description
      "[The FHIT gene is located at the FRA 3B fragile site at chromosome 3p 14.2, and alterations in the FHIT gene and Fhit protein have been found associated with genome instability, particularly in BRCA 2 mutated breast tumours.]. 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:11562178;
    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:NP255651.RAY1WY4PJuPjBN54IE8jzXmuiOb3h3YDgrAFIRlXqURfU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:23+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" .
}