@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0> .
@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:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_head {
  this: np:hasAssertion dgn-np:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_assertion;
    np:hasProvenance dgn-np:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_provenance;
    np:hasPublicationInfo dgn-np:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_assertion a np:Assertion .
  
  dgn-np:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_provenance a np:Provenance .
  
  dgn-np:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_assertion {
  miriam-gene:2678 a ncit:C16612 .
  
  lld:C0008370 a ncit:C7057 .
  
  dgn-gda:DGN2bf1ed329463077791a794d843152ecf sio:SIO_000628 miriam-gene:2678, lld:C0008370;
    a sio:SIO_001121 .
}

dgn-np:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_provenance {
  dgn-np:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_assertion dcterms:description
      "[Defect in ABCB4 function causes the production of bile with low phospholipid content, increased lithogenicity and high detergent properties leading to bile duct luminal membrane injuries and resulting in cholestasis with increased serum gamma-glutamyltransferase (GGT) activity.]. 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:17562004;
    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:NP192044.RABs_D8ei87Lzj69SymewvQupu1ypZ7Sn0RT09H6oEFi0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:45+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" .
}