@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0> .
@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:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_head {
  this: np:hasAssertion dgn-np:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_assertion ;
    np:hasProvenance dgn-np:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_provenance ;
    np:hasPublicationInfo dgn-np:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_assertion a np:Assertion .
  dgn-np:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_provenance a np:Provenance .
  dgn-np:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  lld:C0019243 a ncit:C7057 .
  dgn-gda:DGNd85f67d521102ffa8db6ac803d02347e sio:SIO_000628 miriam-gene:3133 , lld:C0019243 ;
    a sio:SIO_001121 .
}
dgn-np:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_provenance {
  dgn-np:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_assertion dcterms:description "[In order to study if in patients with hereditary angioedema (HAE), copy number of the two genes (C4A and C4A) encoded in the central region of main histocompatibility complex (MHC) influences the diagnostically important C4 serum concentration as well as the clinical course of the disease, we determined copy number of the complement C4A and C4B genes in DNA samples of 95 HAE patients and 246 healthy controls.]. 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:17229465 ;
    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:NP837775.RAGSKahICEVa3fJS1TdTf_VhXlwnOtPd8htP72oLgkk-0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:32+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" .
}