@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU> .
@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:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_head {
  this: np:hasAssertion dgn-np:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_assertion;
    np:hasProvenance dgn-np:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_provenance;
    np:hasPublicationInfo dgn-np:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_assertion a np:Assertion .
  
  dgn-np:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_provenance a np:Provenance .
  
  dgn-np:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_assertion {
  miriam-gene:55997 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN0b0f91cb3787dd9e27aa776c3db8d1d4 sio:SIO_000628 miriam-gene:55997, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_provenance {
  dgn-np:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_assertion dcterms: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: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:NP625084.RAbeTmERCWIkAZCQaZeCmkjLFGm7KL1XcZCfcnSQ9ECDU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:17+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" .
}