@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s> .
@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:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_head {
  this: np:hasAssertion dgn-np:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_assertion;
    np:hasProvenance dgn-np:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_provenance;
    np:hasPublicationInfo dgn-np:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_assertion a np:Assertion .
  
  dgn-np:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_provenance a np:Provenance .
  
  dgn-np:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_assertion {
  miriam-gene:26580 a ncit:C16612 .
  
  lld:C0037772 a ncit:C7057 .
  
  dgn-gda:DGNc8d30cad010d77c092fa1f342ba112c1 sio:SIO_000628 miriam-gene:26580, lld:C0037772;
    a sio:SIO_001121 .
}

dgn-np:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_provenance {
  dgn-np:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_assertion dcterms:description
      "[Further study of the pathological mechanisms of the mutant forms of seipin may lead to important new insights into motor neuron diseases, including other spastic paraplegia diseases and amyotrophic lateral sclerosis.]. 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:18790819;
    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:NP158824.RAcM2XXfERatY_8gK3wjiQOR9cMmte1_DwVNihJ3-iC0s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:25+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" .
}