@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y> .
@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 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:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_head {
  this: np:hasAssertion dgn-np:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_assertion;
    np:hasProvenance dgn-np:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_provenance;
    np:hasPublicationInfo dgn-np:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_assertion a np:Assertion .
  
  dgn-np:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_provenance a np:Provenance .
  
  dgn-np:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_assertion {
  miriam-gene:2525 a ncit:C16612 .
  
  lld:C0577631 a ncit:C7057 .
  
  dgn-gda:DGN72b4911a8c89e5b6d7a7ebc75636ece7 sio:SIO_000628 miriam-gene:2525, lld:C0577631;
    a sio:SIO_001122 .
}

dgn-np:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_provenance {
  dgn-np:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_assertion dct:description
      "[ The lack of a statistically significant association between Lewis 'genotype' and subclinical atherosclerosis in our data suggests that earlier studies reporting associations at the 'phenotypic' level may reflect aspects of the biology of the Lewis system other than an inherent genetic property.]. 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:14687237;
    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:NP43850.RAlRqXE7rRHrSIp1_RB3FwaPmeGTHuHyGLCAXf1hlGl6Y130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}