@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8> .
@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:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_head {
  this: np:hasAssertion dgn-np:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_assertion;
    np:hasProvenance dgn-np:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_provenance;
    np:hasPublicationInfo dgn-np:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_assertion a np:Assertion .
  
  dgn-np:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_provenance a np:Provenance .
  
  dgn-np:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_assertion {
  miriam-gene:5158 a ncit:C16612 .
  
  lld:C0339535 a ncit:C7057 .
  
  dgn-gda:DGN24ccabc0e6ed5846b18d58831aecc6cb sio:SIO_000628 miriam-gene:5158, lld:C0339535;
    a sio:SIO_001121 .
}

dgn-np:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_provenance {
  dgn-np:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_assertion dcterms:description
      "[We have excluded the five previously known mutations in the three genes (RHO, PDE6B and GNAT1) associated with adCSNB, and linkage studies have excluded tight linkage between the disease locus and markers associated with these three genes.]. 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:15845035;
    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:NP663719.RAvjWRMTc0A-UGdN8kCYJq5jFCluY13kYiG9IdFi_L3m8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:41+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" .
}