@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM> .
@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:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_head {
  this: np:hasAssertion dgn-np:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_assertion;
    np:hasProvenance dgn-np:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_provenance;
    np:hasPublicationInfo dgn-np:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_assertion a np:Assertion .
  
  dgn-np:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_provenance a np:Provenance .
  
  dgn-np:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_assertion {
  miriam-gene:65217 a ncit:C16612 .
  
  lld:C2931206 a ncit:C7057 .
  
  dgn-gda:DGN67396b08b3fa87230e8b374d962ce174 sio:SIO_000628 miriam-gene:65217, lld:C2931206;
    a sio:SIO_001121 .
}

dgn-np:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_provenance {
  dgn-np:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_assertion dcterms:description
      "[Mutations in five genes, including MYO7A, USH1C, CDH23, PCDH15 and SANS, have been shown to be the cause of Usher syndrome type 1B, type 1C, type 1D, type 1F and type 1G, respectively.]. 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:15660226;
    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:NP772460.RAlGBhkFREKuHX9GxaSpKpTfDAHVsTeyfO7dsocktRrQM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:47+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" .
}