@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg> .
@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:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_head {
  this: np:hasAssertion dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_assertion;
    np:hasProvenance dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_provenance;
    np:hasPublicationInfo dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_assertion a np:Assertion .
  
  dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_provenance a np:Provenance .
  
  dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0014859 a ncit:C7057 .
  
  dgn-gda:DGN52333764548181922770fc9fadcaa6c8 sio:SIO_000628 miriam-gene:7157, lld:C0014859;
    a sio:SIO_001121 .
}

dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_provenance {
  dgn-np:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_assertion dcterms:description
      "[Our study shows that p53 point mutations occur more frequently in patients with esophageal cancer from this region than in patients from other areas of the world where the disease is prevalent.]. 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:8028358;
    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:NP1330258.RAQ7_G-MHKWif7ejHfulIpwCDjXuhm9JmdUvcLYUweljg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:49+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" .
}