@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM> .
@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:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_head {
  this: np:hasAssertion dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_assertion;
    np:hasProvenance dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_provenance;
    np:hasPublicationInfo dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_assertion a np:Assertion .
  
  dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_provenance a np:Provenance .
  
  dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_assertion {
  miriam-gene:5216 a ncit:C16612 .
  
  lld:C0236642 a ncit:C7057 .
  
  dgn-gda:DGN14b6a48d290ab796424cedeaf8795009 sio:SIO_000628 miriam-gene:5216, lld:C0236642;
    a sio:SIO_001121 .
}

dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_provenance {
  dgn-np:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_assertion dcterms:description
      "[Here, we performed a large screen of US, Nordic, and German familial and sporadic ALS and frontotemporal dementia (FTLD) patients for PFN1 mutations to get further insight into the spectrum and pathogenic relevance of this gene for the complete ALS/FTLD continuum.]. 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:23141414;
    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:NP237885.RAA4nqYnxvP4mzSv5FIUlqqagtWgFeVy-sT1onO8cvcUM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}