@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc> .
@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/v3.0.0/void/> .

dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_head {
  this: np:hasAssertion dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_assertion;
    np:hasProvenance dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_provenance;
    np:hasPublicationInfo dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_assertion a np:Assertion .
  
  dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_provenance a np:Provenance .
  
  dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_assertion {
  miriam-gene:7276 a ncit:C16612 .
  
  lld:C0152025 a ncit:C7057 .
  
  dgn-gda:DGN2cbd6a2cfacb499d6dcfbb84d3b0f5ee sio:SIO_000628 miriam-gene:7276, lld:C0152025;
    a sio:SIO_001121 .
}

dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_provenance {
  dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_assertion dcterms:description
      "[Clinicians should consider, to avoid misdiagnosis, the screening for TTR mutations in patients presenting with progressive axonal polyneuropathy of undetermined etiology, including apparently sporadic cases with pathological examinations negative for amyloid deposition.]. 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:22592564;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:19+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}