@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA> .
@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:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_head {
  this: np:hasAssertion dgn-np:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_assertion;
    np:hasProvenance dgn-np:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_provenance;
    np:hasPublicationInfo dgn-np:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_assertion a np:Assertion .
  
  dgn-np:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_provenance a np:Provenance .
  
  dgn-np:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_assertion {
  miriam-gene:10243 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN80dd4cf6198c83b5b339e61a1a0897ac sio:SIO_000628 miriam-gene:10243, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_provenance {
  dgn-np:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_assertion dcterms:description
      "[The hypermutability and the specific p53 mutations involving the biologically functional domain (e.g., zinc binding domain or DNA contact region) have an insignificant influence on invasive progression in the breast cancer.]. 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:11715068;
    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:NP762494.RAdQ-NOhAFNPb6e-APH7Gm9FbBUVmsS_D6558bfHygbOA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:41+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" .
}