@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk> .
@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:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_head {
  this: np:hasAssertion dgn-np:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_assertion;
    np:hasProvenance dgn-np:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_provenance;
    np:hasPublicationInfo dgn-np:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_assertion a np:Assertion .
  
  dgn-np:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_provenance a np:Provenance .
  
  dgn-np:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_assertion {
  miriam-gene:8195 a ncit:C16612 .
  
  lld:C0265215 a ncit:C7057 .
  
  dgn-gda:DGNcd9ea46bc8f5cb4768619e6486601bdd sio:SIO_000628 miriam-gene:8195, lld:C0265215;
    a sio:SIO_001121 .
}

dgn-np:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_provenance {
  dgn-np:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_assertion dcterms:description
      "[This is the largest and most comprehensive genomic study on MKS in Arabs and the results, in addition to revealing genetic and allelic heterogeneity, suggest that previously reported disease genes and the novel candidates uncovered by this study account for the overwhelming majority of MKS patients in our population.]. 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:23169490;
    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:NP315999.RAkWvsBDhmL3C3796QtOlgQqj1ZTuH2yCaIekCFcIOgNk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:01+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" .
}