@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8> .
@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:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_head {
  this: np:hasAssertion dgn-np:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_assertion;
    np:hasProvenance dgn-np:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_provenance;
    np:hasPublicationInfo dgn-np:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_assertion a np:Assertion .
  
  dgn-np:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_provenance a np:Provenance .
  
  dgn-np:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_assertion {
  miriam-gene:2475 a ncit:C16612 .
  
  lld:C0684249 a ncit:C7057 .
  
  dgn-gda:DGNf10ca3626944a95811b0ba017e110cf9 sio:SIO_000628 miriam-gene:2475, lld:C0684249;
    a sio:SIO_001121 .
}

dgn-np:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_provenance {
  dgn-np:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_assertion dcterms:description
      "[In accordance with the developmental mode of lung cancer established by Sekine et al., we assumed that the occurrence and development of lung cancer were linked not only to gene loss in the 3p region (WNT7A, 3p25) and genetic mutations in the 9p region but also to similar events in the regions of 1p36.2 (FRAP1), 6q25.2-q27 (PARK2), and 11q13 (CCND1).]. 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:23237220;
    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:NP518818.RAMkD3iQtfR4OR0j8lwBg6oUVlhjs6G7gExvTaZAb36U8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:09+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" .
}