@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54> .
@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:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_head {
  this: np:hasAssertion dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_assertion ;
    np:hasProvenance dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_provenance ;
    np:hasPublicationInfo dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_assertion {
  miriam-gene:2261 a ncit:C16612 .
  lld:C0000768 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_provenance {
  dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_assertion dcterms:description "[The number of birth defect cases in the Texas Birth Defects Registry (one of the largest active birth defects surveillance systems in the world) enabled us to examine six different heritable disorders (aqueductal stenosis, infantile polycystic kidney disease, achondroplasia, thanatophoric dwarfism, chondrodysplasia/dwarfism not otherwise specified (NOS), and osteogenesis imperfecta) for a variety of descriptive demographic variables.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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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 .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP600788.RAFh54sgOA1_8EKhA4hgrUsonenJHHs3_WFJjctoJTO54130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:01+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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}