@prefix bfo: <http://purl.obolibrary.org/obo/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE> .
@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 wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_head {
  this: np:hasAssertion dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_assertion;
    np:hasProvenance dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_provenance;
    np:hasPublicationInfo dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_assertion a np:Assertion .
  
  dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_provenance a np:Provenance .
  
  dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_assertion {
  miriam-gene:100528024 a ncit:C16612 .
  
  lld:C0008626 a ncit:C7057 .
  
  dgn-gda:DGNc2df2f95206788e9facfa2922cc1875f sio:SIO_000628 miriam-gene:100528024,
      lld:C0008626;
    a sio:SIO_001121 .
}

dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_provenance {
  dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_assertion dcterms:description
      "[Using 11 DNA markers covering the entire distal region of 11p13, including the WAGR region, we have carried out molecular studies on 58 patients with one or more features of this syndrome and patients with other diseases or structural cytogenetic abnormalities associated with 11p13.]. 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:1769647;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy bfo:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a bfo:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP624772.RAL6UdEGMFULRx7JVvuD_B-3QDmLpzG2pnxcXIVo3tBCE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:28+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}