@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc> .
@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:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_head {
  this: np:hasAssertion dgn-np:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_assertion;
    np:hasProvenance dgn-np:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_provenance;
    np:hasPublicationInfo dgn-np:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_assertion a np:Assertion .
  
  dgn-np:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_provenance a np:Provenance .
  
  dgn-np:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_assertion {
  miriam-gene:5739 a ncit:C16612 .
  
  lld:C0004153 a ncit:C7057 .
  
  dgn-gda:DGN284fe949a16276c2b29a659f37260d36 sio:SIO_000628 miriam-gene:5739, lld:C0004153;
    a sio:SIO_001121 .
}

dgn-np:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_provenance {
  dgn-np:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_assertion dcterms:description
      "[We conclude that for haploinsufficient mutants, such as the R212C, the enhanced atherothrombotic phenotype is likely dependent on the presence of existing atherosclerosis or injury (high risk factors), analogous to what has been observed in the cyclooxygenase-2 inhibition studies or prostacyclin receptor knockout mice studies.]. 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:18323528;
    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:NP895786.RAaH-G_IzRLCSshnuUO5d6R9AWcykSh21Pv0o06bQ3MSc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:10+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" .
}