@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM> .
@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:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_head {
  this: np:hasAssertion dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_assertion ;
    np:hasProvenance dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_provenance ;
    np:hasPublicationInfo dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_assertion a np:Assertion .
  dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_provenance a np:Provenance .
  dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_assertion {
  miriam-gene:4049 a ncit:C16612 .
  lld:C0020459 a ncit:C7057 .
  dgn-gda:DGN5f928bd0828cea5c52c0eb99dd2d56b3 sio:SIO_000628 miriam-gene:4049 , lld:C0020459 ;
    a sio:SIO_001121 .
}
dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_provenance {
  dgn-np:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_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:NP766983.RALBf1jJu6bYx9h5pGApOe1SSsvYfDHh5erPsJRblV0GM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:44+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" .
}