@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI> .
@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:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_head {
  this: np:hasAssertion dgn-np:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_assertion;
    np:hasProvenance dgn-np:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_provenance;
    np:hasPublicationInfo dgn-np:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_assertion a np:Assertion .
  
  dgn-np:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_provenance a np:Provenance .
  
  dgn-np:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_assertion {
  miriam-gene:25797 a ncit:C16612 .
  
  lld:C0036631 a ncit:C7057 .
  
  dgn-gda:DGN0a17cfc66cb59e76665fe66b13870ae3 sio:SIO_000628 miriam-gene:25797, lld:C0036631;
    a sio:SIO_001121 .
}

dgn-np:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_provenance {
  dgn-np:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_assertion dcterms:description
      "[In support of the previous studies, our results demonstrated that LOH on 1p is frequent in both seminomas and NSGCTs, indicating that there is an important tumor suppressor on 1p in GCT.]. 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:11376806;
    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:NP778121.RAzyTEOMCcts2e3lik97CbamB_2Uftr9NDBdSUCpIE8yI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:51+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" .
}