@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_head {
  this: np:hasAssertion dgn-np:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_assertion;
    np:hasProvenance dgn-np:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_provenance;
    np:hasPublicationInfo dgn-np:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_assertion a np:Assertion .
  
  dgn-np:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_provenance a np:Provenance .
  
  dgn-np:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_assertion {
  miriam-gene:2896 a ncit:C16612 .
  
  lld:C1862941 a ncit:C7057 .
  
  dgn-gda:DGNdb88ba2924141fecb1841c2248a78f2e sio:SIO_000628 miriam-gene:2896, lld:C1862941;
    a sio:SIO_001121 .
}

dgn-np:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_provenance {
  dgn-np:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_assertion dcterms:description
      "[The hexanucleotide repeat expansion (GGGGCC) in chromosome 9 open-reading frame 72 (C9orf72) and mutations in the microtubule-associated protein tau (MAPT) and progranulin (GRN) genes are known to be associated with the main causes of familial or sporadic amyotrophic lateral sclerosis and frontotemporal dementia (FTD) in Western populations.]. 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:24387985;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1141627.RApAtdUVTLq-5QOjagSMg1HgX96P_C5N0bEDZen-WrA_k130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:23+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}