@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ> .
@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:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_head {
  this: np:hasAssertion dgn-np:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_assertion;
    np:hasProvenance dgn-np:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_provenance;
    np:hasPublicationInfo dgn-np:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_assertion a np:Assertion .
  
  dgn-np:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_provenance a np:Provenance .
  
  dgn-np:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_assertion {
  miriam-gene:8850 a ncit:C16612 .
  
  lld:C0795907 a ncit:C7057 .
  
  dgn-gda:DGNf7544add6426ae8954f2bb0920750e49 sio:SIO_000628 miriam-gene:8850, lld:C0795907;
    a sio:SIO_001121 .
}

dgn-np:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_provenance {
  dgn-np:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_assertion dcterms:description
      "[To investigate molecular and clinical aspects of conotruncal anomaly face (CAF), we studied the correlation between deletion size and phenotype and the mode of inheritance in 183 conotruncal anomaly face syndrome (CAFS) patients.]. 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:9737780;
    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:NP788340.RAbq-nIa3olJSyvW2Guu5MpBrfSIpv8i8SRHRpNwXPhYQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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" .
}