@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M> .
@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/v3.0.0/void/> .
dgn-np:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_head {
  this: np:hasAssertion dgn-np:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_assertion ;
    np:hasProvenance dgn-np:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_provenance ;
    np:hasPublicationInfo dgn-np:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_assertion a np:Assertion .
  dgn-np:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_provenance a np:Provenance .
  dgn-np:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_assertion {
  miriam-gene:4153 a ncit:C16612 .
  lld:C0024138 a ncit:C7057 .
  dgn-gda:DGN4c7b466442b3d5ad8b03198f23fed8b4 sio:SIO_000628 miriam-gene:4153 , lld:C0024138 ;
    a sio:SIO_001122 .
}
dgn-np:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_provenance {
  dgn-np:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_assertion dcterms:description "[Only in SLE patients fulfilling >/=4 ACR criteria an increased frequency of MBL variant alleles was found. MBL variant alleles were also associated with increased risk of disease activity and of complicating infections indicating that the MBL gene is an S]. 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:11781711 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP69092.RAMRxrV8F-DG-9cXRwlshsNW8-uv1iKVkzVckZRzE046M130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:18+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}