@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo> .
@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:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_head {
  this: np:hasAssertion dgn-np:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_assertion;
    np:hasProvenance dgn-np:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_provenance;
    np:hasPublicationInfo dgn-np:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_assertion a np:Assertion .
  
  dgn-np:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_provenance a np:Provenance .
  
  dgn-np:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_assertion {
  miriam-gene:140913 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGN67c0e3848ee28ffa62cb8ed5270ba1f9 sio:SIO_000628 miriam-gene:140913, lld:C0004096;
    a sio:SIO_001121 .
}

dgn-np:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_provenance {
  dgn-np:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_assertion dcterms:description
      "[CRP single nucleotide polymorphisms (SNPs) did not increase the risk of asthma, but CRP rs1205 CC genotype significantly decreased the predictive value of forced vital capacity (FVC) in the asthma group (adjusted mean change = -7.54%, 95% CI = -13.82 to -1.25%).]. 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:21790705;
    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:NP575878.RAq3kja5J9cBpbMZzCF64KKd8KHIDCMzidJZBGlhS1ruo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:47+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" .
}