@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4> .
@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:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_head {
  this: np:hasAssertion dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_assertion;
    np:hasProvenance dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_provenance;
    np:hasPublicationInfo dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_assertion a np:Assertion .
  
  dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_provenance a np:Provenance .
  
  dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_assertion {
  miriam-gene:2316 a ncit:C16612 .
  
  lld:C0266464 a ncit:C7057 .
  
  dgn-gda:DGN8baa2b76e4eb829b23959b1e78e09716 sio:SIO_000628 miriam-gene:2316, lld:C0266464;
    a sio:SIO_001121 .
}

dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_provenance {
  dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_assertion dcterms:description
      "[We identified 30 patients as having both PNH and PMG on brain imaging, reviewed clinical data and brain imaging studies (or neuropathology summary) for all, and performed mutation analysis of FLNA in nine patients.]. 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:16311271;
    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:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:45+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" .
}