@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA> .
@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:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_head {
  this: np:hasAssertion dgn-np:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_assertion;
    np:hasProvenance dgn-np:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_provenance;
    np:hasPublicationInfo dgn-np:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_assertion a np:Assertion .
  
  dgn-np:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_provenance a np:Provenance .
  
  dgn-np:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0027051 a ncit:C7057 .
  
  dgn-gda:DGN97d44fcbb56123532f0d09f439e86c63 sio:SIO_000628 miriam-gene:3077, lld:C0027051;
    a sio:SIO_001122 .
}

dgn-np:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_provenance {
  dgn-np:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_assertion dcterms:description
      "[In a population of 1279 Caucasians with angiographically confirmed coronary status, there is no evidence of an association between the C282Y mutation in the haemochromatosis gene and prevalence of coronary artery disease and myocardial infarction ]. 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:12746412;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP126341.RARzVc6T6Po9KezIBBMyatSBAgFW4m0EcI_VuZ0dZDgaA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:05+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" .
}