@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw> .
@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:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_head {
  this: np:hasAssertion dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_assertion;
    np:hasProvenance dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_provenance;
    np:hasPublicationInfo dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_assertion a np:Assertion .
  
  dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_provenance a np:Provenance .
  
  dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_assertion {
  miriam-gene:2176 a ncit:C16612 .
  
  lld:C0030297 a ncit:C7057 .
  
  dgn-gda:DGNe4c85ec15cc4550a7c052dcf793397dd sio:SIO_000628 miriam-gene:2176, lld:C0030297;
    a sio:SIO_001121 .
}

dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_provenance {
  dgn-np:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_assertion dcterms:description
      "[Sequence analysis of 38 individuals with familial pancreatic cancer enrolled in the National Familial Pancreatic Tumor Registry (NFPTR) revealed previously identified polymorphisms within two exons and one intron of FANCC, and in three introns of FANCG.]. 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:14726700;
    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:NP584915.RAUO8Yv147xHE4DbB0D52wYZY8HnngDr3RZbpHHv1ynQw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:52+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" .
}