@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs> .
@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/v3.0.0/void/> .

dgn-np:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_head {
  this: np:hasAssertion dgn-np:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_assertion;
    np:hasProvenance dgn-np:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_provenance;
    np:hasPublicationInfo dgn-np:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_assertion a np:Assertion .
  
  dgn-np:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_provenance a np:Provenance .
  
  dgn-np:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_assertion {
  miriam-gene:6990 a ncit:C16612 .
  
  lld:C0339528 a ncit:C7057 .
  
  dgn-gda:DGNa99169e35bfa6996a6fb17517fb3d0a0 sio:SIO_000628 miriam-gene:6990, lld:C0339528;
    a sio:SIO_001121 .
}

dgn-np:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_provenance {
  dgn-np:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_assertion dcterms:description
      "[The RP3 gene, which is responsible for the predominant form of XLRP in most Caucasian populations, has been localized to Xp21.1 by linkage analysis and the map positions of chromosomal deletions associated with the disease.]. 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:8659520;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP726637.RAo5iaZfarBI7WS-4jU3rXmF87XrRw6s4Gir34OqddNhs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:58+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}