@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w> .
@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:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_head {
  this: np:hasAssertion dgn-np:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_assertion;
    np:hasProvenance dgn-np:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_provenance;
    np:hasPublicationInfo dgn-np:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_assertion a np:Assertion .
  
  dgn-np:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_provenance a np:Provenance .
  
  dgn-np:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_assertion {
  miriam-gene:114614 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGNa9906b5ae61890360251cb70a5f307b7 sio:SIO_000628 miriam-gene:114614, lld:C0678222;
    a sio:SIO_001121 .
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dgn-np:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_provenance {
  dgn-np:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_assertion dcterms:description
      "[In addition to creating a catalogue of all mutations and polymorphisms in breast cancer susceptibility genes, a principle aim of the BIC is to facilitate the detection and characterization of these genes by providing technical support in the form of mutation detection protocols, primer sequences, and reagent access.]. 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:10923033;
    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:NP696109.RAouqRAKOYZXxtxmetJiIsqCJyiU_EiCxCFPr8aJv0n9w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:03+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}