@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o> .
@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:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_head {
  this: np:hasAssertion dgn-np:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_assertion;
    np:hasProvenance dgn-np:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_provenance;
    np:hasPublicationInfo dgn-np:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_assertion a np:Assertion .
  
  dgn-np:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_provenance a np:Provenance .
  
  dgn-np:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0007194 a ncit:C7057 .
  
  dgn-gda:DGN7e807766468338d18745be177d81b891 sio:SIO_000628 miriam-gene:3949, lld:C0007194;
    a sio:SIO_001121 .
}

dgn-np:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_provenance {
  dgn-np:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_assertion dcterms:description
      "[Genetic testing and screening in children or adolescents for conditions such as hypertrophic cardiomyopathy (HCM), familial hypercholesterolemia (FH), and long QT (LQT) syndrome, when indicated, can help to save lives through preventive treatment and therapeutic interventions.]. 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:10386275;
    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:NP405228.RA9YHDpGASRrNQTd1bC2PwteXk2h7a7rABTI1np4FYg4o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:01+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" .
}