@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4> .
@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:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_head {
  this: np:hasAssertion dgn-np:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_assertion;
    np:hasProvenance dgn-np:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_provenance;
    np:hasPublicationInfo dgn-np:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_assertion a np:Assertion .
  
  dgn-np:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_provenance a np:Provenance .
  
  dgn-np:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  
  lld:C0271097 a ncit:C7057 .
  
  dgn-gda:DGN872c099ecd61de5bcc9c57200b2b5591 sio:SIO_000628 miriam-gene:2706, lld:C0271097;
    a sio:SIO_001122 .
}

dgn-np:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_provenance {
  dgn-np:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_assertion dcterms:description
      "[Usher syndrome is more prevalent than has been reported before the genome project era. Early diagnosis of Usher syndrome has important positive implications for childhood safety, educational planning, genetic counseling, and treatment. The results demonstrate that DNA testing for Usher syndrome is feasible and may be a useful addition to newborn hearing screening programs.]. 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:20613545;
    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:NP87155.RAv-fbEAlbN3L_DcWDspjYQqtwJ4nFnJNgAKJIhOViKT4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:43+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" .
}