@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8> .
@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:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_head {
  this: np:hasAssertion dgn-np:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_assertion;
    np:hasProvenance dgn-np:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_provenance;
    np:hasPublicationInfo dgn-np:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_assertion a np:Assertion .
  
  dgn-np:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_provenance a np:Provenance .
  
  dgn-np:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C2239176 a ncit:C7057 .
  
  dgn-gda:DGNe8b42d456b431e54c24e817512b9a20e sio:SIO_000628 miriam-gene:7157, lld:C2239176;
    a sio:SIO_001121 .
}

dgn-np:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_provenance {
  dgn-np:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_assertion dcterms:description
      "[These findings suggest that alterations in the p53, p16, and p15 genes are common in human pancreatic cancer cell lines, while p53 or RB mutations are common in hepatoma cell lines.]. 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:9058294;
    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:NP1368662.RAvSLzPk1Nd_EMuvk4QaXj3RNQh9TE4rB_Q-vGywaF7Y8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:06+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" .
}