@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48> .
@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:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_head {
  this: np:hasAssertion dgn-np:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_assertion;
    np:hasProvenance dgn-np:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_provenance;
    np:hasPublicationInfo dgn-np:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_assertion a np:Assertion .
  
  dgn-np:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_provenance a np:Provenance .
  
  dgn-np:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_assertion {
  miriam-gene:9856 a ncit:C16612 .
  
  lld:C1848199 a ncit:C7057 .
  
  dgn-gda:DGNfb680b3be0e600c279fb1ea50ce1f957 sio:SIO_000628 miriam-gene:9856, lld:C1848199;
    a sio:SIO_001121 .
}

dgn-np:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_provenance {
  dgn-np:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_assertion dcterms:description
      "[LIS1 was the first gene cloned that was important for neuronal migration in any organism, and heterozygous mutations or deletions of LIS1 are found in the majority of patients with lissencephaly, while DCX mutations were found in males with X-linked lissencephaly.]. 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:20688183;
    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:NP710345.RAHhsrPShJsSdVPJXR_4xboG51D_nGrQy-cDJrDTw3u48130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:11+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" .
}