@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y> .
@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:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_head {
  this: np:hasAssertion dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_assertion;
    np:hasProvenance dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_provenance;
    np:hasPublicationInfo dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_assertion a np:Assertion .
  
  dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_provenance a np:Provenance .
  
  dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_assertion {
  miriam-gene:9211 a ncit:C16612 .
  
  lld:C0242363 a ncit:C7057 .
  
  dgn-gda:DGNa4a5f8ecc8a79dea9873c9c7f105db39 sio:SIO_000628 miriam-gene:9211, lld:C0242363;
    a sio:SIO_001121 .
}

dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_provenance {
  dgn-np:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_assertion dcterms:description
      "[We have studied 44 benign and malignant EPTs by comparative genomic hybridization to correlate the overall number of genetic alterations with clinical and histopathological parameters and to identify chromosomal regions which might harbor genes involved in EPT pathogenesis and progression.]. 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:10595906;
    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:NP936194.RAhlUyRLQH8Oft72vNh59OvBTYKFfQUcOi1mdtb3orX8Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:33+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" .
}