@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U> .
@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:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_head {
  this: np:hasAssertion dgn-np:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_assertion ;
    np:hasProvenance dgn-np:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_provenance ;
    np:hasPublicationInfo dgn-np:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_assertion a np:Assertion .
  dgn-np:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_provenance a np:Provenance .
  dgn-np:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_assertion {
  miriam-gene:3240 a ncit:C16612 .
  lld:C0162871 a ncit:C7057 .
  dgn-gda:DGN910d739ef2728ea5b1b7969db5a96b94 sio:SIO_000628 miriam-gene:3240 , lld:C0162871 ;
    a sio:SIO_001121 .
}
dgn-np:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_provenance {
  dgn-np:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_assertion dcterms:description "[We have followed up a previous report of a weak association between the haptoglobin 2-1 phenotype and aortic aneurysm and investigated polymorphisms of the haptoglobin gene and neighbouring cholesterol ester transfer protein gene on the long arm of chromosome 16 in patients with atherosclerotic abdominal aortic aneurysm, patients with stenosing aortic atherosclerosis and healthy control subjects.]. 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:1967566 ;
    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:NP844496.RASoIsuuYdMy_Dh-GRV1jInELvPCnC_3t-3sXvqQGBH2U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:36+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" .
}