@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM> .
@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:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_head {
  this: np:hasAssertion dgn-np:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_assertion;
    np:hasProvenance dgn-np:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_provenance;
    np:hasPublicationInfo dgn-np:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_assertion a np:Assertion .
  
  dgn-np:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_provenance a np:Provenance .
  
  dgn-np:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_assertion {
  miriam-gene:1641 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGN665128ca5043280ca79bb647ff344d9a sio:SIO_000628 miriam-gene:1641, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_provenance {
  dgn-np:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_assertion dcterms:description
      "[Whereas the brain malformation due to LIS1 mutations was more severe over the parietal and occipital regions, XLIS mutations produced the reverse gradient, which was more severe over the frontal cortex.]. 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:9817918;
    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:NP261701.RA0fqArrosc-PTXQDBnDTGoVDH_cp4QB_9jUHqv65qbNM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}