@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4> .
@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:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_head {
  this: np:hasAssertion dgn-np:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_assertion ;
    np:hasProvenance dgn-np:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance ;
    np:hasPublicationInfo dgn-np:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_assertion a np:Assertion .
  dgn-np:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance a np:Provenance .
  dgn-np:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_assertion {
  miriam-gene:100130239 a ncit:C16612 .
  lld:C1956346 a ncit:C7057 .
  dgn-gda:DGN9b5ef087d724d2dd80f59882b0278922 sio:SIO_000628 miriam-gene:100130239 , lld:C1956346 ;
    a sio:SIO_001122 .
}
dgn-np:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_provenance {
  dgn-np:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_assertion dcterms:description "[The use of data on genetic variants and the addition of data on global monocytic gene expression led to the identification of the novel functional CAD susceptibility locus LIPA, located on chromosome 10q23.31. The respective eSNPs associated with CAD strongly affect LIPA gene expression level, which was related to endothelial dysfunction, a precursor of 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:21606135 ;
    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:NP96091.RA7svAOkslw1qbXsFm87pqMd8RR6vMdMO3HrIW1EHxvE4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:48+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" .
}