@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw> .
@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:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_head {
  this: np:hasAssertion dgn-np:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_assertion;
    np:hasProvenance dgn-np:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_provenance;
    np:hasPublicationInfo dgn-np:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_assertion a np:Assertion .
  
  dgn-np:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_provenance a np:Provenance .
  
  dgn-np:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_assertion {
  miriam-gene:5827 a ncit:C16612 .
  
  lld:C0007959 a ncit:C7057 .
  
  dgn-gda:DGNfdda9523751e09665685d5f4ffe5e603 sio:SIO_000628 miriam-gene:5827, lld:C0007959;
    a sio:SIO_001121 .
}

dgn-np:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_provenance {
  dgn-np:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_assertion dcterms:description
      "[The 121 patients were selected from 443 possible CMT/HNPP (hereditary neuropathy with liability to pressure palsies) patients based on genetic linkage to Xq13.1, absence of the 17p12 duplication and deletion, and absence of point mutations in PMP22 and P0.]. 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:9099841;
    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:NP1370414.RAgIUQn6nwxw9KgkGcqgSP898f-QRvQV58nkmJMVCF9Aw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:07+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" .
}