@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A> .
@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 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:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_head {
  this: np:hasAssertion dgn-np:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_assertion;
    np:hasProvenance dgn-np:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_provenance;
    np:hasPublicationInfo dgn-np:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_assertion a np:Assertion .
  
  dgn-np:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_provenance a np:Provenance .
  
  dgn-np:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_assertion {
  miriam-gene:55997 a ncit:C16612 .
  
  lld:C0018799 a ncit:C7057 .
  
  dgn-gda:DGNfa00b1b8aad9103b3abbc8dbe4db5ca7 sio:SIO_000628 miriam-gene:55997, lld:C0018799;
    a sio:SIO_001122 .
}

dgn-np:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_provenance {
  dgn-np:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_assertion dc:description
      "[The aim of this study was to identify potential pathological mutations in the Cryptic (CFC1) gene in 500 Chinese children with CHD and to gain insight into the etiology of CHD.]. 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:19853937;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP78084.RAeFOTJ4V9NAfJE9kzsd-4A9oiN1LzXMNZBkTyMeEAS0A130_publicationInfo {
  this: dc:created "2014-10-02T12:32:38+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}