@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg> .
@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/v4.0.0/void/> .

dgn-np:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_head {
  this: np:hasAssertion dgn-np:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_assertion;
    np:hasProvenance dgn-np:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance;
    np:hasPublicationInfo dgn-np:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_assertion a np:Assertion .
  
  dgn-np:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance a np:Provenance .
  
  dgn-np:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_assertion {
  miriam-gene:1641 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN8012d5cdfb8b06abb487424399b2b04a sio:SIO_000628 miriam-gene:1641, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_provenance {
  dgn-np:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_assertion dcterms:description
      "[Lissencephaly caused by LIS1 or DCX mutation frequently results in West syndrome, while lissencephaly due to ARX mutation is associated with the most severe form of epilepsy but never results in West syndrome nor infantile spasms.]. 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:16806828;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP557117.RAlGIrINR0arIaC8Zuf3MS0wvPLT3eI87Dx0Y0rsu9HFg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:57+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" .
}