@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47689.RAfixblYv7fVzgkVOXAbFOelI0eU4Bvc5nrEQpvGnzN-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#> .
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  this: np:hasAssertion dgn-np:NP47689.RAfixblYv7fVzgkVOXAbFOelI0eU4Bvc5nrEQpvGnzN-0130_assertion ;
    np:hasProvenance dgn-np:NP47689.RAfixblYv7fVzgkVOXAbFOelI0eU4Bvc5nrEQpvGnzN-0130_provenance ;
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dgn-np:NP47689.RAfixblYv7fVzgkVOXAbFOelI0eU4Bvc5nrEQpvGnzN-0130_assertion {
  miriam-gene:721 a ncit:C16612 .
  lld:C0007820 a ncit:C7057 .
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dgn-np:NP47689.RAfixblYv7fVzgkVOXAbFOelI0eU4Bvc5nrEQpvGnzN-0130_provenance {
  dgn-np:NP47689.RAfixblYv7fVzgkVOXAbFOelI0eU4Bvc5nrEQpvGnzN-0130_assertion dcterms:description "[ In previous studies C4B*Q0 frequency was reported to be higher in CHD patients aged 45 to 60 years than in aged-matched controls. Moreover, high anti-hsp60 levels were found in CHD patients. These findings contrast with our present report of lower frequency of C4B*Q0 in CVD patients. Therefore, genetic and immunologic factors may at least partly explain the differences between the natural history and risk factors of CHD and CVD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP47689.RAfixblYv7fVzgkVOXAbFOelI0eU4Bvc5nrEQpvGnzN-0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime ;
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