@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE> .
@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:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_head {
  this: np:hasAssertion dgn-np:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_assertion;
    np:hasProvenance dgn-np:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_provenance;
    np:hasPublicationInfo dgn-np:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_assertion a np:Assertion .
  
  dgn-np:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_provenance a np:Provenance .
  
  dgn-np:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_assertion {
  miriam-gene:23435 a ncit:C16612 .
  
  lld:C0497327 a ncit:C7057 .
  
  dgn-gda:DGN0ec78c69a2fc472bb753228ab95d01dc sio:SIO_000628 miriam-gene:23435, lld:C0497327;
    a sio:SIO_001121 .
}

dgn-np:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_provenance {
  dgn-np:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_assertion dcterms:description
      "[TAR-DNA-binding protein 43 (TDP-43), encoded by the TARDBP gene on chromosome 1p36.22, has been identified as the major pathological protein in abnormal inclusions in neurons and glial cells in sporadic amyotrophic lateral sclerosis (SALS), SOD1-negative familial ALS (FALS) and frontotemporal lobar dementia (FTLD).]. 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:19411082;
    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:NP347656.RAOjFte_KX00f3ZPt0gsRvIec8x97Z79kdoisP7JHuRUE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:24+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" .
}