@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak> .
@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:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_head {
  this: np:hasAssertion dgn-np:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_assertion;
    np:hasProvenance dgn-np:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_provenance;
    np:hasPublicationInfo dgn-np:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_assertion a np:Assertion .
  
  dgn-np:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_provenance a np:Provenance .
  
  dgn-np:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_assertion {
  miriam-gene:10648 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN49a6d6fe0ad8374d98195d3a5cb02e9e sio:SIO_000628 miriam-gene:10648, lld:C1956346;
    a sio:SIO_001121 .
}

dgn-np:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_provenance {
  dgn-np:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_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.]. 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: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:NP886866.RAPo_FsFTE5DqE1e8ZiXHePtwDFr44pn5xA17fVKbLIak130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:04+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" .
}