@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg> .
@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:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_head {
  this: np:hasAssertion dgn-np:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_assertion;
    np:hasProvenance dgn-np:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_provenance;
    np:hasPublicationInfo dgn-np:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_assertion a np:Assertion .
  
  dgn-np:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_provenance a np:Provenance .
  
  dgn-np:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_assertion {
  miriam-gene:3240 a ncit:C16612 .
  
  lld:C0010054 a ncit:C7057 .
  
  dgn-gda:DGNc1d99be01b259faa1ef4f0c798a21627 sio:SIO_000628 miriam-gene:3240, lld:C0010054;
    a sio:SIO_001122 .
}

dgn-np:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_provenance {
  dgn-np:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_assertion dcterms:description
      "[Several recent prospective longitudinal studies have demonstrated conflicting results regarding whether there is an increase or decrease in the relative risk of coronary heart disease (CHD) conferred on individuals homozygous for the haptoglobin 1 allele (Hp 1-1).]. 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:15019547;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP57567.RAHOZAp5BOg8P4r8-N7qrdT2rKFvwOXfLtEoV2iQS84gg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}