@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8> .
@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/v3.0.0/void/> .
dgn-np:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_head {
  this: np:hasAssertion dgn-np:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_assertion ;
    np:hasProvenance dgn-np:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_provenance ;
    np:hasPublicationInfo dgn-np:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_assertion a np:Assertion .
  dgn-np:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_provenance a np:Provenance .
  dgn-np:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  lld:C0522055 a ncit:C7057 .
  dgn-gda:DGN9a4dca56e8e8c1141bbaa1e39f40fe40 sio:SIO_000628 miriam-gene:3757 , lld:C0522055 ;
    a sio:SIO_001122 .
}
dgn-np:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_provenance {
  dgn-np:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_assertion dcterms:description "[ In this comprehensive cardiac channel gene screen of the largest cohort of consecutive, unrelated patients referred for LQTS genetic testing, half of the patients had an identifiable mutation. The majority of mutations continue to represent novel singlet]. 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:15840476 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP70210.RA4s28IkonezG8oLNtsh4SpNtuE_5Rq6f5Qf6Z3spbhK8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:18+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}