@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg> .
@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:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_head {
  this: np:hasAssertion dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_assertion;
    np:hasProvenance dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_provenance;
    np:hasPublicationInfo dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_assertion a np:Assertion .
  
  dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_provenance a np:Provenance .
  
  dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0206702 a ncit:C7057 .
  
  dgn-gda:DGN215f21d0cd2bab0d6de399be90973278 sio:SIO_000628 miriam-gene:7157, lld:C0206702;
    a sio:SIO_001121 .
}

dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_provenance {
  dgn-np:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_assertion dcterms:description
      "[The systematic screening for p53 mutations in European patients with hilar cholangiocarcinoma has shown that the type of mutation (except 175) is different and its incidence is much lower when compared to the pattern previously reported for intrahepatic cholangiocarcinoma in East Asian patients.]. 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:10998080;
    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:NP928365.RA3iD4ghh9NXj4yn0bFRHpn_tP7PvFDP3eQEAd2av2Msg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:29+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" .
}