@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ> .
@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:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_head {
  this: np:hasAssertion dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_assertion;
    np:hasProvenance dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_provenance;
    np:hasPublicationInfo dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_assertion a np:Assertion .
  
  dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_provenance a np:Provenance .
  
  dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_assertion {
  miriam-gene:2064 a ncit:C16612 .
  
  lld:C0030186 a ncit:C7057 .
  
  dgn-gda:DGNff236fe6e4ed69d74d0decc2570fd22e sio:SIO_000628 miriam-gene:2064, lld:C0030186;
    a sio:SIO_001121 .
}

dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_provenance {
  dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_assertion dcterms:description
      "[These results suggest the contribution of the HER2 signaling pathway to the pathogenesis and progression of some cases of extramammary Paget's disease, for which clinical use of molecular target therapy against the HER2 pathway is warranted.]. 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:16311120;
    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:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:04+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" .
}