@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ> .
@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:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_head {
  this: np:hasAssertion dgn-np:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion;
    np:hasProvenance dgn-np:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_provenance;
    np:hasPublicationInfo dgn-np:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion a np:Assertion .
  
  dgn-np:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_provenance a np:Provenance .
  
  dgn-np:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion {
  miriam-gene:19 a ncit:C16612 .
  
  lld:C2931838 a ncit:C7057 .
  
  dgn-gda:DGN3d4425da55817d751cfbab5c48cce8b6 sio:SIO_000628 miriam-gene:19, lld:C2931838;
    a sio:SIO_001121 .
}

dgn-np:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_provenance {
  dgn-np:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_assertion dcterms:description
      "[These data show that mutations in ABC1 are the major cause of familial HDL deficiency associated with defective cholesterol efflux, and that CERP has an essential role in the formation of HDL.]. 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:10533863;
    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:NP527730.RAgBsvZJw1FsjFWMbUod3McVu1R20CtqFwU5M4NVQJFiQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:16+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" .
}