@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo> .
@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:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_head {
  this: np:hasAssertion dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_assertion ;
    np:hasProvenance dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_provenance ;
    np:hasPublicationInfo dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_assertion a np:Assertion .
  dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_provenance a np:Provenance .
  dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_assertion {
  miriam-gene:8036 a ncit:C16612 .
  lld:C0028326 a ncit:C7057 .
  dgn-gda:DGN56cf0ec63f097740648fa55c105d52f7 sio:SIO_000628 miriam-gene:8036 , lld:C0028326 ;
    a sio:SIO_001121 .
}
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_provenance {
  dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_assertion dcterms:description "[We reported for the first time a case of 13-year-old boy with NS with loose anagen hair (NSLAH) resulting from mutation in SHOC2 who developed an autoimmune disorder that fulfilled four American College of Rheumatology (ACR) criteria for the classification of SLE (polyarthritis, pericarditis, antinuclear antibodies, and anti-DNA antibodies).]. 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:23786871 ;
    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:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:59+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" .
}