@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_head {
  this: np:hasAssertion dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_assertion;
    np:hasProvenance dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_provenance;
    np:hasPublicationInfo dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_assertion a np:Assertion .
  
  dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_provenance a np:Provenance .
  
  dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_assertion {
  miriam-gene:115761 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN0b8e9ab2c7d01215bc69c04d4c312a84 sio:SIO_000628 miriam-gene:115761, lld:C0006826;
    a sio:SIO_001122 .
}

dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_provenance {
  dgn-np:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_assertion dcterms:description
      "[The ARLTS1 mutation Trp149Stop and Cys148Arg have been shown to be associated with familial cancers, but limited information is available regarding the impact of ARLTS1 variants on familial ovarian cancer (OC).]. 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:19509554;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP965800.RAfD_CVF89kXCh6HM26pvSrbLYWC2YHMFXs96EMPOJCcE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:30+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}