@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4> .
@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:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_head {
  this: np:hasAssertion dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_assertion;
    np:hasProvenance dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_provenance;
    np:hasPublicationInfo dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_assertion a np:Assertion .
  
  dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_provenance a np:Provenance .
  
  dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C1258085 a ncit:C7057 .
  
  dgn-gda:DGN37657051537af98f7280401c98deac11 sio:SIO_000628 miriam-gene:7157, lld:C1258085;
    a sio:SIO_001121 .
}

dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_provenance {
  dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_assertion dcterms:description
      "[Application of these findings to clinical problems include the identification of p53 mutations as markers for malignant change in Barrett's epithelium, the use of discordant p53 mutations to diagnose second primary malignant neoplasms in patients with head and neck cancer, and the potential for therapy by the reversal of genetic lesions.]. 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:1444790;
    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:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:34+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" .
}