@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c> .
@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:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_head {
  this: np:hasAssertion dgn-np:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_assertion;
    np:hasProvenance dgn-np:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_provenance;
    np:hasPublicationInfo dgn-np:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_assertion a np:Assertion .
  
  dgn-np:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_provenance a np:Provenance .
  
  dgn-np:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0206663 a ncit:C7057 .
  
  dgn-gda:DGN0337d7b0bf980f782e483621ee092117 sio:SIO_000628 miriam-gene:1029, lld:C0206663;
    a sio:SIO_001121 .
}

dgn-np:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_provenance {
  dgn-np:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_assertion dcterms:description
      "[To investigate the possible role of this gene in the genesis of the central nervous system primitive neuroectodermal tumor (PNET), four established PNET cell lines and 18 PNET surgical specimens were studied for deletions and mutations of the MTS1/CDKN2 gene.]. 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:7791990;
    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:NP842686.RAPel5xCanOfHHbdDKe0jn0hQz7O17-Qf8aVbCEaoBf9c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:35+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" .
}