@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc> .
@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:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_head {
  this: np:hasAssertion dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_assertion;
    np:hasProvenance dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_provenance;
    np:hasPublicationInfo dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_assertion a np:Assertion .
  
  dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_provenance a np:Provenance .
  
  dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_assertion {
  miriam-gene:768 a ncit:C16612 .
  
  lld:C0334424 a ncit:C7057 .
  
  dgn-gda:DGN380312019287fe60fc0776d45d18f82b sio:SIO_000628 miriam-gene:768, lld:C0334424;
    a sio:SIO_001121 .
}

dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_provenance {
  dgn-np:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_assertion dcterms:description
      "[A well characterized series of nodular melanoma (originally 202 cases) and other benign and malignant melanocytic tumors (109 cases) were examined for the presence of necrosis, apoptotic activity (TUNEL assay), immunohistochemical expression of hypoxia markers (HIF-1 alpha, CAIX, TNF-alpha, Apaf-1) and cell adhesion proteins (alphavbeta3 integrin, CD44/HCAM and osteopontin).]. 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:19061491;
    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:NP489847.RA4QnvGJ8So8Jj6eX2BrGhtSUQnPiFl2bXvlYRKwQZXnc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:52+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" .
}