@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U> .
@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 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:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_head {
  this: np:hasAssertion dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_assertion;
    np:hasProvenance dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_provenance;
    np:hasPublicationInfo dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_assertion a np:Assertion .
  
  dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_provenance a np:Provenance .
  
  dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_assertion {
  miriam-gene:4626 a ncit:C16612 .
  
  lld:C0009081 a ncit:C7057 .
  
  dgn-gda:DGNb31344c5cd2475f2f451e6df302567fa sio:SIO_000628 miriam-gene:4626, lld:C0009081;
    a sio:SIO_001122 .
}

dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_provenance {
  dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_assertion dc:description
      "[This study further differentiates congenital idiopathic clubfoot as distinct from other complex genetic syndromes that can present with similar deformities, and thus facilitates further research to improve the clinical diagnosis and treatment of congenital idiopathic clubfoot.]. 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:20357587;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_publicationInfo {
  this: dc:created "2014-10-02T12:32:41+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}