@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg> .
@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:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_head {
  this: np:hasAssertion dgn-np:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_assertion;
    np:hasProvenance dgn-np:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_provenance;
    np:hasPublicationInfo dgn-np:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_assertion a np:Assertion .
  
  dgn-np:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_provenance a np:Provenance .
  
  dgn-np:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_assertion {
  miriam-gene:4049 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGNdb3aa8f26f529bbb3e1c644c3a6cfa9d sio:SIO_000628 miriam-gene:4049, lld:C0524620;
    a sio:SIO_001121 .
}

dgn-np:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_provenance {
  dgn-np:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_assertion dcterms:description
      "[Homozygosity for rare alleles of the LTA 252A>G polymorphisms was associated with features of metabolic syndrome such as hyperinsulinemia, dyslipidemia, small LDL particle and low adiponectin level in CAD patients, suggesting that CAD patients with LTA 252GG are at high risk and needed an intensive intervention against further progression.]. 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:17640627;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP637346.RAxYzf8HhS3FxPajiP4yCm2ionLsZmBcAOCcHBR2CDnlg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:24+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" .
}