@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw> .
@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:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_head {
  this: np:hasAssertion dgn-np:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_assertion ;
    np:hasProvenance dgn-np:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_provenance ;
    np:hasPublicationInfo dgn-np:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_assertion a np:Assertion .
  dgn-np:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_provenance a np:Provenance .
  dgn-np:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_assertion {
  miriam-gene:7033 a ncit:C16612 .
  lld:C0024266 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_provenance {
  dgn-np:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_assertion dcterms:description "[To assess the difference in genetic aberration patterns among the invasive tumor front (ITF), center/superficiality and the stroma adjacent to oral squamous cell carcinoma (OSCC), we studied loss of heterozygosity (LOH) and microsatellite instability (MI) at chromosome 9p21 and 17p13 on the three regions by combining laser capture microdissection (LCM) and PCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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}
dgn-np:NP189796.RAt6SA_OzhwvLfFLVvK210qRwaSo4HKofugilMTRJ4dxw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:44+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
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}