@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM> .
@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:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_head {
  this: np:hasAssertion dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_assertion ;
    np:hasProvenance dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_provenance ;
    np:hasPublicationInfo dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_assertion a np:Assertion .
  dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_provenance a np:Provenance .
  dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_assertion {
  miriam-gene:717 a ncit:C16612 .
  lld:C0242383 a ncit:C7057 .
  dgn-gda:DGN56cd6a32d5616f1f8d55f60197790ca8 sio:SIO_000628 miriam-gene:717 , lld:C0242383 ;
    a sio:SIO_001122 .
}
dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_provenance {
  dgn-np:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_assertion dcterms:description "[The HDL-raising allele of the LIPC gene (T) was associated with a reduced risk of AMD. Higher total cholesterol and LDL levels were associated with increased risk, whereas higher HDL levels tended to reduce the risk of AMD. The specific mechanisms underlying the association between AMD and LIPC require further investigation.]. 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:20888482 ;
    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:NP63833.RA9OC22gNJRvIWdOojKeYPwKxijg-EnpMnS5sEGYO38VM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}