@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8> .
@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:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_head {
  this: np:hasAssertion dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_assertion;
    np:hasProvenance dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_provenance;
    np:hasPublicationInfo dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_assertion a np:Assertion .
  
  dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_provenance a np:Provenance .
  
  dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_assertion {
  miriam-gene:8856 a ncit:C16612 .
  
  lld:C0751783 a ncit:C7057 .
  
  dgn-gda:DGN558085ce6c15d6957974110ddde3a7e4 sio:SIO_000628 miriam-gene:8856, lld:C0751783;
    a sio:SIO_001121 .
}

dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_provenance {
  dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_assertion dcterms:description
      "[The most abundant PXR alternative mRNA transcripts lacked 111 nucleotides, deleting 37 amino acids from the PXR LBD (PXR.2), or lacked 123 nt, deleting 41 amino acids from the PXR LBD (PXR.3).]. 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:15364541;
    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:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:20+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" .
}