@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ> .
@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/v4.0.0/void/> .

dgn-np:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_head {
  this: np:hasAssertion dgn-np:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_assertion;
    np:hasProvenance dgn-np:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_provenance;
    np:hasPublicationInfo dgn-np:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_assertion a np:Assertion .
  
  dgn-np:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_provenance a np:Provenance .
  
  dgn-np:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_assertion {
  miriam-gene:7353 a ncit:C16612 .
  
  lld:C0039685 a ncit:C7057 .
  
  dgn-gda:DGNf30f948544b9a9c1e55d58525b8c9942 sio:SIO_000628 miriam-gene:7353, lld:C0039685;
    a sio:SIO_001121 .
}

dgn-np:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_provenance {
  dgn-np:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_assertion dcterms:description
      "[Our data suggest that, although the UFD1L gene is mapped to 22q11 and is expressed during early murine development at both cardiac and cranial neural crests, it is not responsible for the majority of tetralogy of Fallot cases in humans.]. 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:11485030;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP325847.RAVJ43L3PaXbhHoS5GoyBUv1v2JDQf9P5u1CIKDFVyVAQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:13+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}