@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ> .
@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:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_head {
  this: np:hasAssertion dgn-np:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_assertion;
    np:hasProvenance dgn-np:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_provenance;
    np:hasPublicationInfo dgn-np:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_assertion a np:Assertion .
  
  dgn-np:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_provenance a np:Provenance .
  
  dgn-np:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_assertion {
  miriam-gene:4851 a ncit:C16612 .
  
  lld:C0162872 a ncit:C7057 .
  
  dgn-gda:DGN6b7a46fb658434b2037230e4b8f6f514 sio:SIO_000628 miriam-gene:4851, lld:C0162872;
    a sio:SIO_001121 .
}

dgn-np:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_provenance {
  dgn-np:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_assertion dcterms:description
      "[We, therefore, investigated the potential relationship between mutations in regions of NOTCH1 recently reported to be associated with bicuspid aortic valve and the phenotype of bicuspid aortic valve and thoracic aortic aneurysms in unrelated patients undergoing surgical repair.]. 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:17662764;
    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:NP164024.RAD_6NP-luLlvbVmzP85r6OAszglltMwKG0xk6vNkeHeQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}