@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA> .
@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:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_head {
  this: np:hasAssertion dgn-np:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_assertion;
    np:hasProvenance dgn-np:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_provenance;
    np:hasPublicationInfo dgn-np:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_assertion a np:Assertion .
  
  dgn-np:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_provenance a np:Provenance .
  
  dgn-np:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_assertion {
  miriam-gene:4975 a ncit:C16612 .
  
  lld:C0271097 a ncit:C7057 .
  
  dgn-gda:DGNe2e44816a6c458befa8785113f38aa0e sio:SIO_000628 miriam-gene:4975, lld:C0271097;
    a sio:SIO_001121 .
}

dgn-np:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_provenance {
  dgn-np:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_assertion dcterms:description
      "[DNA samples from 59 individuals including parents and affected and nonaffected sibs were typed for markers on chromosomes 1q and 11q for which linkage has recently been established for Usher syndrome types II and I. Statistically significant linkage was observed with four markers on 11q (D11S533, D11S527, OMP, and INT2) with a maximum six-point location score of 11.61 at the D11S533 locus.]. 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:8020954;
    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:NP261589.RAS-ePztUA1WQGGuRJnY3QiAwI0RS0ikdkbId5OEflEZA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}