@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo> .
@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:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_head {
  this: np:hasAssertion dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_assertion;
    np:hasProvenance dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_provenance;
    np:hasPublicationInfo dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_assertion a np:Assertion .
  
  dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_provenance a np:Provenance .
  
  dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_assertion {
  miriam-gene:5551 a ncit:C16612 .
  
  lld:C0206180 a ncit:C7057 .
  
  dgn-gda:DGN7c18de0c76c0e246acb4e9678bfe07d9 sio:SIO_000628 miriam-gene:5551, lld:C0206180;
    a sio:SIO_001121 .
}

dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_provenance {
  dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_assertion dcterms:description
      "[Overall, the incidence of PRF1 mutations was found to be significantly higher in patients with ALCL compared with 400 control subjects, among whom only heterozygous A91V was observed in 41 subjects (10.2%) (chi-square test, 10.9; P <.01).]. 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:17477373;
    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:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:46+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" .
}