@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8> .
@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:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_head {
  this: np:hasAssertion dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_assertion;
    np:hasProvenance dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_provenance;
    np:hasPublicationInfo dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_assertion a np:Assertion .
  
  dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_provenance a np:Provenance .
  
  dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_assertion {
  miriam-gene:4088 a ncit:C16612 .
  
  lld:C0029410 a ncit:C7057 .
  
  dgn-gda:DGNc328435c0a838b460c09999e8739505d sio:SIO_000628 miriam-gene:4088, lld:C0029410;
    a sio:SIO_001121 .
}

dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_provenance {
  dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_assertion dcterms:description
      "[Our data indicate that genetic variation in the SMAD3 gene is involved in the risk of both hip OA and knee OA in European populations, confirming the results from animal models on the potential importance of this molecule in the pathogenesis of OA.]. 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:20506137;
    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:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:47+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" .
}