@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM> .
@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:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_head {
  this: np:hasAssertion dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_assertion;
    np:hasProvenance dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_provenance;
    np:hasPublicationInfo dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_assertion a np:Assertion .
  
  dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_provenance a np:Provenance .
  
  dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_assertion {
  miriam-gene:5376 a ncit:C16612 .
  
  lld:C0700251 a ncit:C7057 .
  
  dgn-gda:DGN041bcd05d71f72fa84bb3665f0749f25 sio:SIO_000628 miriam-gene:5376, lld:C0700251;
    a sio:SIO_001121 .
}

dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_provenance {
  dgn-np:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_assertion dcterms:description
      "[To determine whether hereditary neuropathy with liability to pressure palsies (HNPP) and inherited brachial plexus neuropathy (IBPN) are genetically distinct disorders and to evaluate the usefulness of fluorescence in situ hybridization (FISH) for diagnosing HNPP in individual patients.]. 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:7630211;
    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:NP486252.RADoLXQ3p5Bxd9V_PhbvAl6r7fijO1vGktxf9E0ikNzmM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:50+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" .
}