@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68> .
@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:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_head {
  this: np:hasAssertion dgn-np:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_assertion;
    np:hasProvenance dgn-np:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_provenance;
    np:hasPublicationInfo dgn-np:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_assertion a np:Assertion .
  
  dgn-np:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_provenance a np:Provenance .
  
  dgn-np:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_assertion {
  miriam-gene:2521 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGN6c7fc328d0964524556dd15b2a99ccc5 sio:SIO_000628 miriam-gene:2521, lld:C0002736;
    a sio:SIO_001121 .
}

dgn-np:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_provenance {
  dgn-np:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_assertion dcterms:description
      "[Our findings provide an overview of the occurrence of FUS mutations in Chinese sporadic and familial ALS cases and highlight the importance of screening for FUS mutations in ALS patients of Chinese origin.]. 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:22340366;
    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:NP961299.RA6SwTSqOubpAKxD2fPb8Z6p-X2K9Ap40DAc134WJvY68130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:00+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" .
}