@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w> .
@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:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_head {
  this: np:hasAssertion dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_assertion;
    np:hasProvenance dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_provenance;
    np:hasPublicationInfo dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_assertion a np:Assertion .
  
  dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_provenance a np:Provenance .
  
  dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0038868 a ncit:C7057 .
  
  dgn-gda:DGN260661d280ce2c37a05ee84ca0d19550 sio:SIO_000628 miriam-gene:4137, lld:C0038868;
    a sio:SIO_001121 .
}

dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_provenance {
  dgn-np:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_assertion dcterms:description
      "[Recent studies have reported high familial aggregation in PSP patients, and it has been widely demonstrated that Microtuble Associated Protein Tau (MAPT) gene mutations are causative of monogenic autosomal dominant PSP.]. 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:21568901;
    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:NP893889.RAS-AKz0zVFXsiOiL5odHfcJZimSWBXWds5V7pydS2A-w130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:29+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" .
}