@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA> .
@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:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_head {
  this: np:hasAssertion dgn-np:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_assertion;
    np:hasProvenance dgn-np:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_provenance;
    np:hasPublicationInfo dgn-np:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_assertion a np:Assertion .
  
  dgn-np:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_provenance a np:Provenance .
  
  dgn-np:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_assertion {
  miriam-gene:23022 a ncit:C16612 .
  
  lld:C0235974 a ncit:C7057 .
  
  dgn-gda:DGN55e2fcd383e3f71f5f419d93c7a25cb5 sio:SIO_000628 miriam-gene:23022, lld:C0235974;
    a sio:SIO_001121 .
}

dgn-np:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_provenance {
  dgn-np:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_assertion dcterms:description
      "[These observations suggest that the presence of an abnormal palladin gene in familial pancreatic cancer and the overexpression of palladin protein in sporadic pancreatic cancer cause cytoskeletal changes in pancreatic cancer and may be responsible for or contribute to the tumor's strong invasive and migratory abilities.]. 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:17194196;
    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:NP664212.RAnGhbcfqECVaCPt7Q4yjv9Zl0lbQdHIUL77ib2kWcbCA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:41+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" .
}