@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I> .
@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:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_head {
  this: np:hasAssertion dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_assertion;
    np:hasProvenance dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_provenance;
    np:hasPublicationInfo dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_assertion a np:Assertion .
  
  dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_provenance a np:Provenance .
  
  dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_assertion {
  miriam-gene:1030 a ncit:C16612 .
  
  lld:C0004114 a ncit:C7057 .
  
  dgn-gda:DGNa316dbaebb2a9501f6c4b400c7bd20b6 sio:SIO_000628 miriam-gene:1030, lld:C0004114;
    a sio:SIO_001121 .
}

dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_provenance {
  dgn-np:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_assertion dcterms:description
      "[In a series of 46 glioblastomas, 16 anaplastic astrocytomas and eight astrocytomas, all tumours retaining one or both alleles of CDKN2A (48 tumours) and CDKN2B (49 tumours) were subjected to sequence analysis (entire coding region and splice acceptor and donor sites).]. 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:9000591;
    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:NP881323.RACG1Dnr226MD2MM4vOojtuWwlDVg5jMUnudOOmAPoW7I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:58+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" .
}