@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE> .
@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:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_head {
  this: np:hasAssertion dgn-np:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_assertion;
    np:hasProvenance dgn-np:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_provenance;
    np:hasPublicationInfo dgn-np:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_assertion a np:Assertion .
  
  dgn-np:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_provenance a np:Provenance .
  
  dgn-np:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0041408 a ncit:C7057 .
  
  dgn-gda:DGN82bcd65caca0b4d82b24b7c5af92845d sio:SIO_000628 miriam-gene:1029, lld:C0041408;
    a sio:SIO_001121 .
}

dgn-np:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_provenance {
  dgn-np:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_assertion dcterms:description
      "[The karyotype was abnormal in nine cases, including seven cases of aneuploidy (one Turner syndrome, three trisomy 18, and three trisomy 21) and two cases of structural chromosomal abnormalities (46,XX, del 4 p16.1 and 46,XX, dup1).]. 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:14691994;
    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:NP327885.RAVqADLpV6zRrpuiCBHr7LxQOnLJyo6aDSwXuUr0bYiLE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:13+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: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" .
}