@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo> .
@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:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_head {
  this: np:hasAssertion dgn-np:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_assertion;
    np:hasProvenance dgn-np:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_provenance;
    np:hasPublicationInfo dgn-np:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_assertion a np:Assertion .
  
  dgn-np:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_provenance a np:Provenance .
  
  dgn-np:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_assertion {
  miriam-gene:3690 a ncit:C16612 .
  
  lld:C0151744 a ncit:C7057 .
  
  dgn-gda:DGN8b90ad181aef02cf430d0084618add2a sio:SIO_000628 miriam-gene:3690, lld:C0151744;
    a sio:SIO_001122 .
}

dgn-np:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_provenance {
  dgn-np:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_assertion dcterms:description
      "[We have studied structure of polymorphisms of genes of blood clotting factors II, V, VII, platelet membrane glycoprotein IIIa (GPIIIa) and enzyme methylenetetrahydrofolate reductase (MTHFR) in patients with ischemic heart disease (IHD).]. 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:19463111;
    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:NP55677.RAQjca1xu6bGq1_T1j7E4clQMUEiWXHsqM_vZC8RsCebo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}