@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o> .
@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:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_head {
  this: np:hasAssertion dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_assertion ;
    np:hasProvenance dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_provenance ;
    np:hasPublicationInfo dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_assertion a np:Assertion .
  dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_provenance a np:Provenance .
  dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  lld:C0027651 a ncit:C7057 .
  dgn-gda:DGN809a9b4a7cfc6d9f8a1868bbdfebf9e0 sio:SIO_000628 miriam-gene:1956 , lld:C0027651 ;
    a sio:SIO_001121 .
}
dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_provenance {
  dgn-np:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_assertion dcterms:description "[The histopathologic features of 10 myxoid adrenocortical neoplasms were analyzed, and epidermal growth factor receptor (EGFR) expression, EGFR gene copy number, and EGFR gene mutations in the 10 tumors were detected by using immunohistochemical analysis, fluorescence in situ hybridization, and the Scorpion Amplification Refractory Mutation System (DxS, Manchester, England), respectively.]. 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:22031318 ;
    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:NP307392.RAznh54sSIZPuB4pkfTttewA9o4lOpFqn0DcjmXzVAy1o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:56+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" .
}