@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g> .
@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:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_head {
  this: np:hasAssertion dgn-np:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_assertion;
    np:hasProvenance dgn-np:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_provenance;
    np:hasPublicationInfo dgn-np:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_assertion a np:Assertion .
  
  dgn-np:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_provenance a np:Provenance .
  
  dgn-np:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNc8bf0954e998e3245e2078e3bb254384 sio:SIO_000628 miriam-gene:675, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_provenance {
  dgn-np:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_assertion dcterms:description
      "[One major difference is that in the United States, Myriad Genetics is the sole provider of genetic testing, because it has sole control of relevant patents for BRCA1 and BRCA2 genes, whereas genetic testing for familial colorectal cancer is available from multiple laboratories.]. 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:20393305;
    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:NP339509.RAAElPBbGXYwa8MSNX0MqnwhSk8zFAVJcU42jC0U50i1g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:19+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" .
}