@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_head {
  this: np:hasAssertion dgn-np:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_assertion;
    np:hasProvenance dgn-np:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_provenance;
    np:hasPublicationInfo dgn-np:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_assertion a np:Assertion .
  
  dgn-np:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_provenance a np:Provenance .
  
  dgn-np:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0027962 a ncit:C7057 .
  
  dgn-gda:DGNa8c3411e61d7c8713452cde387486f59 sio:SIO_000628 miriam-gene:1029, lld:C0027962;
    a sio:SIO_001121 .
}

dgn-np:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_provenance {
  dgn-np:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_assertion dcterms:description
      "[All the childhood melanoma cases were associated with loss of p16 without any correlation with their Breslow thickness whereas all the Spitz nevi and benign melanocytic nevi had strong positive nuclear and cytoplasmic expression of p16 staining.]. 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:21550132;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP892319.RAEX0mX_Gj6rn1IjDqMcpvdZ4h7uEhZFqILw44DmxP4X0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:28+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}