@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4> .
@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:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_head {
  this: np:hasAssertion dgn-np:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_assertion;
    np:hasProvenance dgn-np:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_provenance;
    np:hasPublicationInfo dgn-np:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_assertion a np:Assertion .
  
  dgn-np:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_provenance a np:Provenance .
  
  dgn-np:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_assertion {
  miriam-gene:3207 a ncit:C16612 .
  
  lld:C1456781 a ncit:C7057 .
  
  dgn-gda:DGNf37a53c9b8503215c2854f8f6f7c2f20 sio:SIO_000628 miriam-gene:3207, lld:C1456781;
    a sio:SIO_001121 .
}

dgn-np:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_provenance {
  dgn-np:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_assertion dcterms:description
      "[We found that the expression levels of HOXA11, A13, B9, D12 and D13 in melanoma were higher than those in nevus pigmentosus and that the expression levels of HOXA11, B2 and C13 were significantly different between pT4 melanoma and pT1 to pT3 melanoma.]. 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:15551325;
    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:NP497577.RADNmwESURZC0tdx31I0fv5yRUafAlSY4Rj8vKR74UDT4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:57+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" .
}