@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI> .
@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:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_head {
  this: np:hasAssertion dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_assertion;
    np:hasProvenance dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_provenance;
    np:hasPublicationInfo dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_assertion a np:Assertion .
  
  dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_provenance a np:Provenance .
  
  dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_assertion {
  miriam-gene:727 a ncit:C16612 .
  
  lld:C0343713 a ncit:C7057 .
  
  dgn-gda:DGNd0af05045f3b4048ce95bee172b31a70 sio:SIO_000628 miriam-gene:727, lld:C0343713;
    a sio:SIO_001121 .
}

dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_provenance {
  dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_assertion dcterms:description
      "[Absence of the fifth component of complement (C5) by immunochemical assay and marked deficiency by hemolytic assay (less than 0.1%) was found in a family in which the oldest male child had suffered severe and recurrent meningococcemia at age 15 years, two brothers developed meningococcal meningitis four years later (at ages 18 and 14 years), and a sister had the gonococcal arthritis-dermatitis syndrome.]. 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:6785713;
    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:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:17+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" .
}