@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ> .
@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:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_head {
  this: np:hasAssertion dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_assertion;
    np:hasProvenance dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_provenance;
    np:hasPublicationInfo dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_assertion a np:Assertion .
  
  dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_provenance a np:Provenance .
  
  dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_assertion {
  miriam-gene:24 a ncit:C16612 .
  
  lld:C0015397 a ncit:C7057 .
  
  dgn-gda:DGN368e47b7b1bb626b5b3955612120e99a sio:SIO_000628 miriam-gene:24, lld:C0015397;
    a sio:SIO_001121 .
}

dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_provenance {
  dgn-np:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_assertion dcterms:description
      "[Screening of increasingly large numbers of patients would help to determine whether this can be explained by ethnic differences, or is an indicator of extensive allelic heterogeneity of ABCR in STGD1 and other eye diseases.]. 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:10711710;
    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:NP183098.RAXzPJUwGKvHaPBv5Mr6bCL27HBz8jXQy6zutekl8q5VQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:39+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" .
}