@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM> .
@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:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_head {
  this: np:hasAssertion dgn-np:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_assertion;
    np:hasProvenance dgn-np:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_provenance;
    np:hasPublicationInfo dgn-np:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_assertion a np:Assertion .
  
  dgn-np:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_provenance a np:Provenance .
  
  dgn-np:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_assertion {
  miriam-gene:6794 a ncit:C16612 .
  
  lld:C0007130 a ncit:C7057 .
  
  dgn-gda:DGN3768e1b55962284be0ed946a96883371 sio:SIO_000628 miriam-gene:6794, lld:C0007130;
    a sio:SIO_001121 .
}

dgn-np:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_provenance {
  dgn-np:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_assertion dcterms:description
      "[These results suggest that mutations in the STK11 gene may play an important role in the etiology of MDA of the uterine cervix and may distinguish this rare tumor from other common types of adenocarcinoma of the uterine cervix.]. 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:12533684;
    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:NP197023.RAVJlK06xRnJSVSU5QsmMFTnFs82DFFAHcE4H1CU8NocM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:48+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" .
}