@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA> .
@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:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_head {
  this: np:hasAssertion dgn-np:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_assertion;
    np:hasProvenance dgn-np:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_provenance;
    np:hasPublicationInfo dgn-np:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_assertion a np:Assertion .
  
  dgn-np:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_provenance a np:Provenance .
  
  dgn-np:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_assertion {
  miriam-gene:4908 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGN7a41c9d210609f471058f73f582f8312 sio:SIO_000628 miriam-gene:4908, lld:C0002736;
    a sio:SIO_001121 .
}

dgn-np:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_provenance {
  dgn-np:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_assertion dcterms:description
      "[Our results suggest that this treatment modality of intrathecal transplantation of human NSCs genetically modified to overexpress neurotrophic factor(s) might be of value in the treatment of ALS patients without significant adverse effects.]. 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:19626053;
    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:NP218559.RA7d1Y1P0xfaZbyYXUiIbHfFL6RDAv26l4K_jVrf2EKbA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:01+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" .
}