@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM> .
@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:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_head {
  this: np:hasAssertion dgn-np:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_assertion;
    np:hasProvenance dgn-np:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_provenance;
    np:hasPublicationInfo dgn-np:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_assertion a np:Assertion .
  
  dgn-np:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_provenance a np:Provenance .
  
  dgn-np:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_assertion {
  miriam-gene:7276 a ncit:C16612 .
  
  lld:C0206245 a ncit:C7057 .
  
  dgn-gda:DGN46cec3451b3e44e4c5d6a15daf1026c8 sio:SIO_000628 miriam-gene:7276, lld:C0206245;
    a sio:SIO_001121 .
}

dgn-np:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_provenance {
  dgn-np:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_assertion dcterms:description
      "[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. 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:23797140;
    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:NP199053.RAVevFtB1DbE_lez9dZU5A7kru5Jg5lYokF3aUYQD1YuM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:49+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" .
}