@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o> .
@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:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_head {
  this: np:hasAssertion dgn-np:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_assertion ;
    np:hasProvenance dgn-np:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_provenance ;
    np:hasPublicationInfo dgn-np:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_assertion a np:Assertion .
  dgn-np:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_provenance a np:Provenance .
  dgn-np:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  lld:C0010606 a ncit:C7057 .
  dgn-gda:DGN670f08fb0c4cd277d8d22300e54fb49f sio:SIO_000628 miriam-gene:3342 , lld:C0010606 ;
    a sio:SIO_001121 .
}
dgn-np:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_provenance {
  dgn-np:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_assertion dcterms:description "[In order to find common genetic abnormalities that may identify loci of genes involved in the development of adenoid cystic carcinoma (ACC), we investigated DNA copy number changes in 24 of these tumors by comparative genomic hybridization (CGH).]. 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:11494110 ;
    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:NP769421.RAK7QVnqNKihpHTzu_Wq3xqTc9QwSEx04Cqmz44L6T44o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:45+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" .
}