@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8> .
@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:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_head {
  this: np:hasAssertion dgn-np:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_assertion;
    np:hasProvenance dgn-np:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_provenance;
    np:hasPublicationInfo dgn-np:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_assertion a np:Assertion .
  
  dgn-np:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_provenance a np:Provenance .
  
  dgn-np:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0031269 a ncit:C7057 .
  
  dgn-gda:DGNbd50ebab097aa881dcdc140f653157be sio:SIO_000628 miriam-gene:675, lld:C0031269;
    a sio:SIO_001121 .
}

dgn-np:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_provenance {
  dgn-np:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_assertion dcterms:description
      "[Germline mutations in BRCA2 have been shown to predispose to both breast and pancreatic cancer, germline mutations in p16 to melanoma and pancreatic cancer (the FAMMM syndrome), and genetic mutations in STK11/LKB1 to pancreatic cancer in patients with the Peutz-Jeghers Syndrome (PJS).]. 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:10436789;
    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:NP277909.RAZiLlTr68bD44KrSOKh83I_LSoM_gaMD3US653zHh_H8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:36+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" .
}