@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw> .
@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:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_head {
  this: np:hasAssertion dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_assertion;
    np:hasProvenance dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_provenance;
    np:hasPublicationInfo dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_assertion a np:Assertion .
  
  dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_provenance a np:Provenance .
  
  dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0162534 a ncit:C7057 .
  
  dgn-gda:DGN6e5802ea7dee5ac2a4f864d7f9563bae sio:SIO_000628 miriam-gene:5621, lld:C0162534;
    a sio:SIO_001121 .
}

dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_provenance {
  dgn-np:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_assertion dcterms:description
      "[The codon for the methionine at position 129 (M129) in the human prion protein provides an alternative initiation site for translation and renders individuals homozygous for M129 more susceptible to prion disease.]. 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:16081222;
    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:NP507441.RAXDMXftJFJzeG-qQvkNn2nDfaUiHEou_IOUzefhHkWqw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:35+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" .
}