@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY> .
@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:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_head {
  this: np:hasAssertion dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_assertion;
    np:hasProvenance dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_provenance;
    np:hasPublicationInfo dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_assertion a np:Assertion .
  
  dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_provenance a np:Provenance .
  
  dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_assertion {
  miriam-gene:7846 a ncit:C16612 .
  
  lld:C0266470 a ncit:C7057 .
  
  dgn-gda:DGNb910544a3ffbdd1b725b509682ce79a6 sio:SIO_000628 miriam-gene:7846, lld:C0266470;
    a sio:SIO_001121 .
}

dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_provenance {
  dgn-np:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_assertion dcterms:description
      "[All together, it emerges that the TUBA1A related lissencephaly spectrum ranges from perisylvian pachygyria, in the less severe form, to posteriorly predominant pachygyria in the most severe, associated with dysgenesis of the anterior limb of the internal capsule and mild to severe cerebellar hypoplasia.]. 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:18728072;
    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:NP826472.RA7k0FDcufrJoI96MuRSM7rrfl2_cdmMb3FhHpL1SCkHY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:26+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" .
}