@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g> .
@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:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_head {
  this: np:hasAssertion dgn-np:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_assertion ;
    np:hasProvenance dgn-np:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_provenance ;
    np:hasPublicationInfo dgn-np:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_assertion a np:Assertion .
  dgn-np:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_provenance a np:Provenance .
  dgn-np:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_assertion {
  miriam-gene:7033 a ncit:C16612 .
  lld:C0007137 a ncit:C7057 .
  dgn-gda:DGNad5cb86a2c0b929a5ea02d31a7d370e6 sio:SIO_000628 miriam-gene:7033 , lld:C0007137 ;
    a sio:SIO_001121 .
}
dgn-np:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_provenance {
  dgn-np:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_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 ;
    sio:SIO_000772 miriam-pubmed:16455286 ;
    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:NP886571.RAFy7_DWO3T-Q0JLdkttSRo0l0WUrWPioW5n7L7Qbo01g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:01+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> ;
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}