@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs> .
@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:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_head {
  this: np:hasAssertion dgn-np:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_assertion;
    np:hasProvenance dgn-np:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_provenance;
    np:hasPublicationInfo dgn-np:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_assertion a np:Assertion .
  
  dgn-np:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_provenance a np:Provenance .
  
  dgn-np:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_assertion {
  miriam-gene:727738 a ncit:C16612 .
  
  lld:C0007114 a ncit:C7057 .
  
  dgn-gda:DGN9d50fc247c47a38ba96826bc87c86827 sio:SIO_000628 miriam-gene:727738, lld:C0007114;
    a sio:SIO_001121 .
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dgn-np:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_provenance {
  dgn-np:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_assertion dcterms:description
      "[Taken together, we propose a novel mechanism by which HuR regulates the stability of AREG mRNA in keratinocytes after UVB exposure and suggest that targeting of HuR functions might be crucial for understanding skin cancers caused by aberrant EGF family member-EGFR signaling.]. 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:23430747;
    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:NP787063.RA_Menori3IO9mYD8frXJjgF-PiNIGsblZhoV41KhLdJs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}