@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8> .
@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:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_head {
  this: np:hasAssertion dgn-np:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_assertion;
    np:hasProvenance dgn-np:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_provenance;
    np:hasPublicationInfo dgn-np:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_assertion a np:Assertion .
  
  dgn-np:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_provenance a np:Provenance .
  
  dgn-np:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_assertion {
  miriam-gene:7276 a ncit:C16612 .
  
  lld:C0031117 a ncit:C7057 .
  
  dgn-gda:DGN1c57dbe120e4bacb232cef60f0e8b0e5 sio:SIO_000628 miriam-gene:7276, lld:C0031117;
    a sio:SIO_001121 .
}

dgn-np:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_provenance {
  dgn-np:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_assertion dcterms:description
      "[Because leptomeningeal amyloidosis occurs in FAP ATTR Val30 Met as the progression of the disease, this information suggests that in addition to peripheral neuropathy, disorders of the central nervous system (CNS) should be given an attention in patients who underwent sequential liver transplantation using an explanted FAP ATTR Val30 Met patient's liver.]. 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:11477356;
    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:NP264714.RA9MLSUB5tFoChsYk0pnai_sv7wqld6GOyzsmBayL0Dg8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}