@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo> .
@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:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_head {
  this: np:hasAssertion dgn-np:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_assertion;
    np:hasProvenance dgn-np:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_provenance;
    np:hasPublicationInfo dgn-np:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_assertion a np:Assertion .
  
  dgn-np:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_provenance a np:Provenance .
  
  dgn-np:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_assertion {
  miriam-gene:78987 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGNf977afc3193fdc04a938f301e03650e8 sio:SIO_000628 miriam-gene:78987, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_provenance {
  dgn-np:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_assertion dcterms:description
      "[Of the several genes identified for CHD, CRELD1 is an important cell adhesion molecule crucial in cardiac development, which is known to cause atrioventricular septal defect in Down syndrome and also in sporadic forms of atrioventricular septal defect.]. 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:21413875;
    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:NP725960.RAhQeiFGDmozL9ua7uzabGDh4WDbcZ_9QhVC0l0k5chVo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:20+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" .
}