@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_head {
  this: np:hasAssertion dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_assertion;
    np:hasProvenance dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_provenance;
    np:hasPublicationInfo dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_assertion a np:Assertion .
  
  dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_provenance a np:Provenance .
  
  dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_assertion {
  miriam-gene:7399 a ncit:C16612 .
  
  lld:C0271097 a ncit:C7057 .
  
  dgn-gda:DGNde1fcb243b7bd25239457f5d3e6cefe7 sio:SIO_000628 miriam-gene:7399, lld:C0271097;
    a sio:SIO_001121 .
}

dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_provenance {
  dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_assertion dcterms:description
      "[Our results indicate that mutations in the USH2A gene and the resulting phenotype are probably modulated by other variables, such as modifying genes, epigenetics or environmental factors which may be of importance for better understanding the etiology of Usher 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:24160897;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:15+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}