@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ> .
@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:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_head {
  this: np:hasAssertion dgn-np:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_assertion ;
    np:hasProvenance dgn-np:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_assertion a np:Assertion .
  dgn-np:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_provenance a np:Provenance .
  dgn-np:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_assertion {
  miriam-gene:712 a ncit:C16612 .
  lld:C0024138 a ncit:C7057 .
  dgn-gda:DGN1024d908fca67f06d733dd6d1ca0a4c9 sio:SIO_000628 miriam-gene:712 , lld:C0024138 ;
    a sio:SIO_001122 .
}
dgn-np:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_provenance {
  dgn-np:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_assertion dcterms:description "[The identification of new mutation in C1qA gene that disrupts the start codon (ATG to AGG (Met1Arg)) has not been reported previously and it expands the knowledge and importance of the C1q gene in the pathogenesis of lupus especially in the high-risk African-American population.]. 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:22472776 ;
    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:NP972342.RAtTBOMkWhnVHNdxjOO-SKyv0011vPkafCde8nAv-NiWQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:05+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" .
}