@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI> .
@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:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_head {
   this: np:hasAssertion dgn-np:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_assertion ;
    np:hasProvenance dgn-np:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_provenance ;
    np:hasPublicationInfo dgn-np:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_assertion a np:Assertion .
  dgn-np:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_provenance a np:Provenance .
  dgn-np:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_assertion {
   miriam-gene:3753 a ncit:C16612 .
  lld:C0232197 a ncit:C7057 .
  dgn-gda:DGNffba79b5259bd53972961f3db9886b09 sio:SIO_000628 miriam-gene:3753 , lld:C0232197 ;
    a sio:SIO_001121 .
}
dgn-np:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_provenance {
   dgn-np:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_assertion dcterms:description "[The minor allele frequencies of P448R, R519H, G643S for KCNQ1 and G38S and D85N for KCNE1 in the AF group, the community control group and the ward control group were 9.9, 7.9, 9.3%; 0, 0, -; 4.3, 4.2, 1.7%; 28.4, 31.7, 29.7%; 0.7, 0.4%, -, respectively.]. 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:17016049 ;
    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:NP382733.RAWictr2uNQl1MTFhezq36eTaSjPRyiHH8ndOxG7pMeyI130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:46+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" .
}