@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ> .
@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:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_head {
  this: np:hasAssertion dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_assertion;
    np:hasProvenance dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_provenance;
    np:hasPublicationInfo dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_assertion a np:Assertion .
  
  dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_provenance a np:Provenance .
  
  dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_assertion {
  miriam-gene:7276 a ncit:C16612 .
  
  lld:C0032580 a ncit:C7057 .
  
  dgn-gda:DGN3452ca6aec688958ba381d264681e3c9 sio:SIO_000628 miriam-gene:7276, lld:C0032580;
    a sio:SIO_001121 .
}

dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_provenance {
  dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_assertion dcterms:description
      "[Although TTR mutations were mostly associated with familial amyloid polyneuropathy (FAP), these molecular variants were also found in patients with recurrent stroke, subarachnoidal bleeding and radiological findings of cerebral, cerebellar, cortical-subcortical infarctions and hemosiderosis.]. 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:19428025;
    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:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:19+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}