@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc> .
@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:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_head {
  this: np:hasAssertion dgn-np:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_assertion;
    np:hasProvenance dgn-np:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_provenance;
    np:hasPublicationInfo dgn-np:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_assertion a np:Assertion .
  
  dgn-np:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_provenance a np:Provenance .
  
  dgn-np:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_assertion {
  miriam-gene:6298 a ncit:C16612 .
  
  lld:C2931822 a ncit:C7057 .
  
  dgn-gda:DGNa3fc500e6f10a2ed398fc2887c56a701 sio:SIO_000628 miriam-gene:6298, lld:C2931822;
    a sio:SIO_001121 .
}

dgn-np:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_provenance {
  dgn-np:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_assertion dcterms:description
      "[Since p16/MTS1, a potential tumor suppressor gene, whose mutations/deletions are frequently found in variety of tumor cells, was mapped to chromosome 9p21, we investigated the possible involvement of this gene in the development of NPC by mutational and Northern blot analysis.]. 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:7862458;
    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:NP504441.RAbLGtm8RBAA8fbCugwMqs-HlAiYeE87vUutbCQCDjkcc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:00+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" .
}