@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP236624.RA1pLTHNEJstlQc4Ouin5rxi2keEmnSl1-2ICA_SDcNq8> .
@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:NP236624.RA1pLTHNEJstlQc4Ouin5rxi2keEmnSl1-2ICA_SDcNq8130_head {
  this: np:hasAssertion dgn-np:NP236624.RA1pLTHNEJstlQc4Ouin5rxi2keEmnSl1-2ICA_SDcNq8130_assertion ;
    np:hasProvenance dgn-np:NP236624.RA1pLTHNEJstlQc4Ouin5rxi2keEmnSl1-2ICA_SDcNq8130_provenance ;
    np:hasPublicationInfo dgn-np:NP236624.RA1pLTHNEJstlQc4Ouin5rxi2keEmnSl1-2ICA_SDcNq8130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP236624.RA1pLTHNEJstlQc4Ouin5rxi2keEmnSl1-2ICA_SDcNq8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP236624.RA1pLTHNEJstlQc4Ouin5rxi2keEmnSl1-2ICA_SDcNq8130_assertion {
  miriam-gene:55636 a ncit:C16612 .
  lld:C0011053 a ncit:C7057 .
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}
dgn-np:NP236624.RA1pLTHNEJstlQc4Ouin5rxi2keEmnSl1-2ICA_SDcNq8130_provenance {
  dgn-np:NP236624.RA1pLTHNEJstlQc4Ouin5rxi2keEmnSl1-2ICA_SDcNq8130_assertion dcterms:description "[These optimised parameters were then applied to an MRI screen of embryos heterozygous for the gene Chd7, implicated in coloboma of the eye, heart defects, atresia of the choanae, retardation of growth, genital/urinary abnormalities, ear abnormalities and deafness (CHARGE) syndrome (a condition partly characterised by cardiovascular birth defects in humans).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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}
dgn-np:NP236624.RA1pLTHNEJstlQc4Ouin5rxi2keEmnSl1-2ICA_SDcNq8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:12+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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