@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY> .
@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:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_head {
  this: np:hasAssertion dgn-np:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_assertion;
    np:hasProvenance dgn-np:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_provenance;
    np:hasPublicationInfo dgn-np:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_assertion a np:Assertion .
  
  dgn-np:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_provenance a np:Provenance .
  
  dgn-np:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_assertion {
  miriam-gene:57045 a ncit:C16612 .
  
  lld:C0007137 a ncit:C7057 .
  
  dgn-gda:DGNec7f12cf51b5068045e93b177b6a0d72 sio:SIO_000628 miriam-gene:57045, lld:C0007137;
    a sio:SIO_001121 .
}

dgn-np:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_provenance {
  dgn-np:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_assertion dcterms:description
      "[Loss of heterozygosity (LOH) has been frequently detected at chromosome 7q31 region in human head and neck squamous cell carcinomas (HNSCC) and many other cancers, suggesting the existence of tumor suppressor genes (TSG).]. 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:12080476;
    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:NP640685.RAyr1t6pZmLI43lQIrjdsKjoa0kod5rtMkhVFrkZ7ZYKY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:26+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" .
}