@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA> .
@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:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_head {
  this: np:hasAssertion dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_assertion;
    np:hasProvenance dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_provenance;
    np:hasPublicationInfo dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_assertion a np:Assertion .
  
  dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_provenance a np:Provenance .
  
  dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0023055 a ncit:C7057 .
  
  dgn-gda:DGN8b505477d5e15a04f05de1c4a226a07e sio:SIO_000628 miriam-gene:3342, lld:C0023055;
    a sio:SIO_001121 .
}

dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_provenance {
  dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_assertion dcterms:description
      "[Our recent comparative genomic hybridization (CGH) study has shown that losses of the long arm of chromosome 13 were the most common aberrations in primary larynx tumors and their corresponding metastases.]. 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:12377414;
    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:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:29+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" .
}