@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0> .
@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:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_head {
  this: np:hasAssertion dgn-np:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_assertion;
    np:hasProvenance dgn-np:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_provenance;
    np:hasPublicationInfo dgn-np:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_assertion a np:Assertion .
  
  dgn-np:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_provenance a np:Provenance .
  
  dgn-np:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_assertion {
  miriam-gene:1571 a ncit:C16612 .
  
  lld:C2931822 a ncit:C7057 .
  
  dgn-gda:DGN7fc5d8266f2c0f55eea08fd6f25bc8f0 sio:SIO_000628 miriam-gene:1571, lld:C2931822;
    a sio:SIO_001121 .
}

dgn-np:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_provenance {
  dgn-np:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_assertion dcterms:description
      "[The higher RR found for the same genotype in distinct populations confirmed that CYP2E1 is one of several NPC susceptibility genes and that the RsaI minus variant is one mutation that affects phenotype.]. 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:11389775;
    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:NP660343.RAjsUi_KNWEWEw8JXjjLLX9PrIoWlLBtoz5aQs5bH_Ak0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}