@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw> .
@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 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:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_head {
  this: np:hasAssertion dgn-np:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_assertion;
    np:hasProvenance dgn-np:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_provenance;
    np:hasPublicationInfo dgn-np:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_assertion a np:Assertion .
  
  dgn-np:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_provenance a np:Provenance .
  
  dgn-np:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_assertion {
  miriam-gene:10599 a ncit:C16612 .
  
  lld:C0020435 a ncit:C7057 .
  
  dgn-gda:DGNca627c5690878238970eeaaf0f050c1c sio:SIO_000628 miriam-gene:10599, lld:C0020435;
    a sio:SIO_001122 .
}

dgn-np:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_provenance {
  dgn-np:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_assertion dct:description
      "[this expanded panel of mutations and polymorphisms can serve as an effective instrument to study the genetic architecture of hyperbilirubinemia and speculate an important role for genetic polymorphism coinheritance in determining hyperbilirubinemia risk i]. 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:18558634;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP81606.RAzgi24lOSvAsBBvgg0EbQpFP8eYrUJeWkZ-pLgTBVDWw130_publicationInfo {
  this: dct:created "2014-10-02T12:32:40+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}