@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc> .
@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:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_head {
  this: np:hasAssertion dgn-np:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_assertion;
    np:hasProvenance dgn-np:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_provenance;
    np:hasPublicationInfo dgn-np:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_assertion a np:Assertion .
  
  dgn-np:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_provenance a np:Provenance .
  
  dgn-np:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_assertion {
  miriam-gene:4087 a ncit:C16612 .
  
  lld:C0677886 a ncit:C7057 .
  
  dgn-gda:DGN6b4952c1330ecff0bd0bb89677f94f96 sio:SIO_000628 miriam-gene:4087, lld:C0677886;
    a sio:SIO_001121 .
}

dgn-np:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_provenance {
  dgn-np:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_assertion dcterms:description
      "[Thus, we propose that the frequent allelic loss at 18q is because of the effect of multiple genes, and there is at least one as yet unidentified tumor suppressor gene at 18q residing distal to SMAD4, SMAD2, and DCC involved in serous ovarian carcinoma.]. 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:11438451;
    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:NP190294.RAMk8qh0zOXcKiKAwrbs-xPKTAksy_eEKXTeYR8DkkLPc130_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;
    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" .
}