@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ> .
@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:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_head {
   this: np:hasAssertion dgn-np:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_assertion ;
    np:hasProvenance dgn-np:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_assertion a np:Assertion .
  dgn-np:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_provenance a np:Provenance .
  dgn-np:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_assertion {
   miriam-gene:5320 a ncit:C16612 .
  lld:C0004153 a ncit:C7057 .
  dgn-gda:DGNbd4c1af63df650046c6066451a09758b sio:SIO_000628 miriam-gene:5320 , lld:C0004153 ;
    a sio:SIO_001121 .
}
dgn-np:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_provenance {
   dgn-np:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_assertion dcterms:description "[The aim of this study was to investigate the molecular mechanism for changes in proteoglycan binding and LDL receptor affinity on two compositional changes in LDL that have been associated with atherosclerosis: cholesterol enrichment of the core and modification by secretory group IIA phospholipase A2 (sPLA2) of the surface.]. 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:14726411 ;
    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:NP749521.RAThtck_kT8x2XJLSf0UmvfC7McuPpGS7HvM4mquCEUCQ130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:34+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" .
}