@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg> .
@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:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_head {
  this: np:hasAssertion dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_assertion;
    np:hasProvenance dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_provenance;
    np:hasPublicationInfo dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_assertion a np:Assertion .
  
  dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_provenance a np:Provenance .
  
  dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_assertion {
  miriam-gene:185 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN18c731a1cf8626ca96cac29650e6d1ab sio:SIO_000628 miriam-gene:185, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_provenance {
  dgn-np:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_assertion dct:description
      "[Six SNPs that were discovered and were associated with CAD may help in explaining the molecular basis of the disorder and the susceptibility to coronary atherosclerosis. It can also help identify early prediction, prevention and therapy for CAD.]. 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:21119571;
    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:NP48857.RAi1CxtXc7Xej4i2Xo2uvkapnGfKlF4UnuiA4o2mr_brg130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+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" .
}