@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ> .
@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:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_head {
  this: np:hasAssertion dgn-np:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_assertion;
    np:hasProvenance dgn-np:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_provenance;
    np:hasPublicationInfo dgn-np:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_assertion a np:Assertion .
  
  dgn-np:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_provenance a np:Provenance .
  
  dgn-np:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN186694de9703eef6ad50b63149437a03 sio:SIO_000628 miriam-gene:675, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_provenance {
  dgn-np:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_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:NP360104.RAHntyVA06g7t5nQB5ztAAcpFfZVpAG0Uwi2R1A_7DemQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:31+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" .
}