@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw> .
@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:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_head {
  this: np:hasAssertion dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_assertion;
    np:hasProvenance dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_provenance;
    np:hasPublicationInfo dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_assertion a np:Assertion .
  
  dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_provenance a np:Provenance .
  
  dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_assertion {
  miriam-gene:100188848 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN1672121d5b6b2d095edeeb1c3c403d76 sio:SIO_000628 miriam-gene:100188848,
      lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_provenance {
  dgn-np:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_assertion dcterms:description
      "[Interestingly, mossy fiber sprouting was less pronounced in patients with FMTLE, suggesting that, when compared to SMTLE, patients with FMTLE respond differently to plastic changes plausibly induced by cell loss, neuronal deafferentation, or epileptic seizures.]. 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:18294201;
    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:NP807360.RAlidUJzPyf2TU9gnwFPYiOcH2_98RiKTbCWBxNwsalDw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:15+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" .
}