@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4> .
@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:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_head {
  this: np:hasAssertion dgn-np:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_assertion;
    np:hasProvenance dgn-np:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_provenance;
    np:hasPublicationInfo dgn-np:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_assertion a np:Assertion .
  
  dgn-np:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_provenance a np:Provenance .
  
  dgn-np:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_assertion {
  miriam-gene:80339 a ncit:C16612 .
  
  lld:C3241937 a ncit:C7057 .
  
  dgn-gda:DGN9614e735581eac95b30a6bdbd69937b2 sio:SIO_000628 miriam-gene:80339, lld:C3241937;
    a sio:SIO_001121 .
}

dgn-np:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_provenance {
  dgn-np:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_assertion dcterms:description
      "[Herein, we aimed to study the association between hepatic fat accumulation as assessed by magnetic resonance imaging and circulating levels of cytokeratin-18 (CK-18) fragments, a robust NASH biomarker, and to explore the impact on this association of ethnicity, insulin resistance, and single nucleotide polymorphisms (SNPs) associated with steatosis (rs738409 in the PNPLA3, rs1260326 in the GCKR) or NASH severity (rs2645424 in the FDFT1).]. 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:23275357;
    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:NP586526.RASlDkSnfrvWY0dW_QB1ocDm8fUfDLSWtyUL4RRlR2ua4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:53+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" .
}