@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88> .
@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:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_head {
  this: np:hasAssertion dgn-np:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_assertion;
    np:hasProvenance dgn-np:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_provenance;
    np:hasPublicationInfo dgn-np:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_assertion a np:Assertion .
  
  dgn-np:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_provenance a np:Provenance .
  
  dgn-np:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN1fcb90629db279fdb82c5687a363b005 sio:SIO_000628 miriam-gene:7248, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_provenance {
  dgn-np:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_assertion dcterms:description
      "[For this study, given the disrupted family backgrounds of many of our patients and the unreliability of family histories, our hypothesis was that in comparison with other samples, family history of coronary heart disease would be a poor screening tool for the identification of children with elevations in total serum cholesterol (TSC).]. 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:8265303;
    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:NP748608.RAPiFBegUvi5pU3jp881cZmHX3gLNkO4Bp0L-KQbBnP88130_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" .
}