@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA> .
@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:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_head {
  this: np:hasAssertion dgn-np:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_assertion;
    np:hasProvenance dgn-np:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_provenance;
    np:hasPublicationInfo dgn-np:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_assertion a np:Assertion .
  
  dgn-np:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_provenance a np:Provenance .
  
  dgn-np:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_assertion {
  miriam-gene:999 a ncit:C16612 .
  
  lld:C0030186 a ncit:C7057 .
  
  dgn-gda:DGNc80ff0dc73614b5600607e1817e581a1 sio:SIO_000628 miriam-gene:999, lld:C0030186;
    a sio:SIO_001121 .
}

dgn-np:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_provenance {
  dgn-np:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_assertion dcterms:description
      "[Therefore, we analyzed the possible mutations in the KRAS, HRAS, NRAS, BRAF, ARAF, RAF1, PIK3CA, AKT1, CTNNB1 and APC genes as well as methylation and expression of CDH1 in 144 EMPD cases and 42 matched normal skin tissues.]. 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:22821211;
    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:NP922457.RACJvQF1GfoZURxW7OOJo0ma0e1BswBDHV5dSUFxiOwkA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:26+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" .
}