@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_head {
  this: np:hasAssertion dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_assertion;
    np:hasProvenance dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_provenance;
    np:hasPublicationInfo dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_assertion a np:Assertion .
  
  dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_provenance a np:Provenance .
  
  dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_assertion {
  miriam-gene:2132 a ncit:C16612 .
  
  lld:C0029423 a ncit:C7057 .
  
  dgn-gda:DGN39e2b47adff2d922acd0bf49feef49ef sio:SIO_000628 miriam-gene:2132, lld:C0029423;
    a sio:SIO_001121 .
}

dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_provenance {
  dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_assertion dcterms:description
      "[Although both benign conditions have been linked to defects in EXT1 or EXT2 genes, contradictory reports are present in the literature regarding the requirement of their biallelic inactivation for osteochondroma development.]. 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:20418910;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:51+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}