@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg> .
@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:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_head {
  this: np:hasAssertion dgn-np:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_assertion;
    np:hasProvenance dgn-np:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_provenance;
    np:hasPublicationInfo dgn-np:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_assertion a np:Assertion .
  
  dgn-np:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_provenance a np:Provenance .
  
  dgn-np:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_assertion {
  miriam-gene:585 a ncit:C16612 .
  
  lld:C0752166 a ncit:C7057 .
  
  dgn-gda:DGNa725ade9f9088d74be7d64a55990400b sio:SIO_000628 miriam-gene:585, lld:C0752166;
    a sio:SIO_001121 .
}

dgn-np:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_provenance {
  dgn-np:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_assertion dcterms:description
      "[The disorder showed statistically significant genetic linkage to the BBS4 locus on chromosome 15 in the affected siblings in two of the families, but the clinical features in these patients did not differ from the other cases of Bardet-Biedl syndrome.]. 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:9227203;
    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:NP534757.RAt_tOMci0TWveWcTuqoLOtzIngRsdXwuhnxbcIYMh3Kg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:23+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" .
}