@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_head {
  this: np:hasAssertion dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_assertion ;
    np:hasProvenance dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_provenance ;
    np:hasPublicationInfo dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_assertion a np:Assertion .
  dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_provenance a np:Provenance .
  dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_assertion {
  miriam-gene:337 a ncit:C16612 .
  lld:C0010054 a ncit:C7057 .
  dgn-gda:DGNefcb27b17f264b0c7f8505301f307f6c sio:SIO_000628 miriam-gene:337 , lld:C0010054 ;
    a sio:SIO_001122 .
}
dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_provenance {
  dgn-np:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_assertion dcterms:description "[Together with previous studies our results indicate that the relation between apo(a) genotypes, Lp(a) levels, and CHD may be heterogeneous across ethnic groups and that it depends on the genetic architecture of the Lp(a) trait in a given population whethe]. 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:12860258 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP80647.RAta_0DNMICNM03NM70gbYAnTtTByNJ8e7XimqCJPI6jA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:24+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}