@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU> .
@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:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_head {
  this: np:hasAssertion dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_assertion;
    np:hasProvenance dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_provenance;
    np:hasPublicationInfo dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_assertion a np:Assertion .
  
  dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_provenance a np:Provenance .
  
  dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGN86fda33d06f458791ef4c426f2fce301 sio:SIO_000628 miriam-gene:675, lld:C0032580;
    a sio:SIO_001121 .
}

dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_provenance {
  dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_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-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:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:46+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" .
}