@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs> .
@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:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_head {
  this: np:hasAssertion dgn-np:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_assertion;
    np:hasProvenance dgn-np:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_provenance;
    np:hasPublicationInfo dgn-np:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_assertion a np:Assertion .
  
  dgn-np:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_provenance a np:Provenance .
  
  dgn-np:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_assertion {
  miriam-gene:2176 a ncit:C16612 .
  
  lld:C0030297 a ncit:C7057 .
  
  dgn-gda:DGN0ce217b997cc427e450583d495e0fdb8 sio:SIO_000628 miriam-gene:2176, lld:C0030297;
    a sio:SIO_001121 .
}

dgn-np:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_provenance {
  dgn-np:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_assertion dcterms:description
      "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. 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:15695377;
    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:NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:30+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" .
}