@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw> .
@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:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_head {
  this: np:hasAssertion dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_assertion;
    np:hasProvenance dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_provenance;
    np:hasPublicationInfo dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_assertion a np:Assertion .
  
  dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_provenance a np:Provenance .
  
  dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_assertion {
  miriam-gene:345 a ncit:C16612 .
  
  lld:C0242339 a ncit:C7057 .
  
  dgn-gda:DGN53ab6b8febd02033af63a0af786b06bb sio:SIO_000628 miriam-gene:345, lld:C0242339;
    a sio:SIO_001121 .
}

dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_provenance {
  dgn-np:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_assertion dcterms:description
      "[The T-455C and C-482T APOC3 promoter region polymorphisms (SNPs) have recently been reported to predispose to dyslipidemia, insulin resistance, and nonalcoholic fatty liver disease (NAFLD) in Indian subjects, but the association with liver damage has not been evaluated so far.]. 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:21777557;
    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:NP569301.RAVemelhraxg3OOIH-IQvKrTjHbssviOSQ1WNDOWFI_dw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:43+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" .
}