@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs> .
@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:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_head {
  this: np:hasAssertion dgn-np:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_assertion;
    np:hasProvenance dgn-np:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_provenance;
    np:hasPublicationInfo dgn-np:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_assertion a np:Assertion .
  
  dgn-np:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_provenance a np:Provenance .
  
  dgn-np:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_assertion {
  miriam-gene:11146 a ncit:C16612 .
  
  lld:C0002726 a ncit:C7057 .
  
  dgn-gda:DGN98f9ed2cae34abe2d51a5882396dc5c5 sio:SIO_000628 miriam-gene:11146, lld:C0002726;
    a sio:SIO_001121 .
}

dgn-np:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_provenance {
  dgn-np:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_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:NP864971.RAgtLIJlJFF1vm05TtpNUbICWu6bpI_PSCeHicqiFTYVs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:48+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" .
}