@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA> .
@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/> .
@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/v3.0.0/void/> .

dgn-np:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_head {
  this: np:hasAssertion dgn-np:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_assertion;
    np:hasProvenance dgn-np:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_provenance;
    np:hasPublicationInfo dgn-np:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_assertion a np:Assertion .
  
  dgn-np:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_provenance a np:Provenance .
  
  dgn-np:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_assertion {
  miriam-gene:1778 a ncit:C16612 .
  
  lld:C1955869 a ncit:C7057 .
  
  dgn-gda:DGN96452612aa53bd0ab8e3169783890faa sio:SIO_000628 miriam-gene:1778, lld:C1955869;
    a sio:SIO_001121 .
}

dgn-np:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_provenance {
  dgn-np:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_assertion dcterms:description
      "[Inputs from genetic studies were provided through the identification of several mutated genes encoding either proteins associated with microtubules (DCX, LIS1, KIF2A, KIF5C, DYNC1H1) or tubulin subunits (TUBA1A, TUBB2B, TUBB5 and TUBG1), in malformations of cortical development (MCD).]. 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:24179174;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP356984.RAypHnSHhBlPlpNbRoW7_UL8Cm5wzlc8CKFRubSJ1VdSA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:06+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}