@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg> .
@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:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_head {
  this: np:hasAssertion dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_assertion;
    np:hasProvenance dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_provenance;
    np:hasPublicationInfo dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_assertion a np:Assertion .
  
  dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_provenance a np:Provenance .
  
  dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_assertion {
  miriam-gene:4942 a ncit:C16612 .
  
  lld:C0266526 a ncit:C7057 .
  
  dgn-gda:DGN84a6f405ccaad68161f2ce0fbe070e1f sio:SIO_000628 miriam-gene:4942, lld:C0266526;
    a sio:SIO_001121 .
}

dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_provenance {
  dgn-np:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_assertion dcterms:description
      "[These results suggest that one of the OAT-related sequences on the X chromosome may be in close proximity to the Norrie disease locus and represent the first report which indicates that the OAT cDNA may be useful for the identification of carrier status and/or prenatal diagnosis.]. 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:2568328;
    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:NP601368.RAPnFetgZ58lqME24v8T_WpxclkfXb5kp7PxaPhzo92tg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:39+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" .
}