@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY> .
@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:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_head {
  this: np:hasAssertion dgn-np:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_assertion;
    np:hasProvenance dgn-np:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_provenance;
    np:hasPublicationInfo dgn-np:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_assertion a np:Assertion .
  
  dgn-np:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_provenance a np:Provenance .
  
  dgn-np:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_assertion {
  miriam-gene:350 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGNc3323017a52200216b18f6948f1f1728 sio:SIO_000628 miriam-gene:350, lld:C0024141;
    a sio:SIO_001122 .
}

dgn-np:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_provenance {
  dgn-np:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_assertion dcterms:description
      "[ The prevalence of mutations in the fifth domain of beta2GPI in these patients with SLE and/or APS were similar to those previously reported for the general population. Heterozygosity for either mutation does not influence the incidence of aPL, but in patients with SLE, the mutation at exon 8 may predispose to thrombosis as an independent factor.]. 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:10366111;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP48077.RAYBllXbIuWt02WIwejmDsrHTFw8OCUgEVeOk2dIPITmY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}