@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk> .
@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/v4.0.0/void/> .

dgn-np:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_head {
  this: np:hasAssertion dgn-np:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_assertion;
    np:hasProvenance dgn-np:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_provenance;
    np:hasPublicationInfo dgn-np:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_assertion a np:Assertion .
  
  dgn-np:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_provenance a np:Provenance .
  
  dgn-np:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGNf9569baf6497553b9310d09d6b4bba19 sio:SIO_000628 miriam-gene:324, lld:C0032580;
    a sio:SIO_001121 .
}

dgn-np:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_provenance {
  dgn-np:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_assertion dcterms:description
      "[As the first effort, we have created a novel variant database of BRCA1 and BRCA2, mismatch repair genes (MMR), and APC genes for breast cancer, Lynch syndrome, and familial adenomatous polyposis (FAP), respectively, in the Chinese population using the Leiden Open Variation Database (LOVD) format.]. 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:21901790;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP922252.RAKHO5ZcXbSy4a7O7fRbLt2a8WRtEDrVancH2z_HiO2hk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:42+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}