@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk> .
@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:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_head {
  this: np:hasAssertion dgn-np:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_assertion;
    np:hasProvenance dgn-np:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_provenance;
    np:hasPublicationInfo dgn-np:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_assertion a np:Assertion .
  
  dgn-np:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_provenance a np:Provenance .
  
  dgn-np:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  
  lld:C2751492 a ncit:C7057 .
  
  dgn-gda:DGN99e4684c9f93401ffc9af7c96ad00991 sio:SIO_000628 miriam-gene:3918, lld:C2751492;
    a sio:SIO_001121 .
}

dgn-np:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_provenance {
  dgn-np:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_assertion dcterms:description
      "[To perform qualitative analysis of variant TTR in CSF of patients who underwent a sequential liver transplantation using an explanted familial amyloidotic polyneuropathy (FAP) ATTR Val30 Met patient's liver, levels and forms of TTR of the two patients were analyzed by means of enzyme linked immunosorbent assay (ELISA) and matrix-assisted laser desorption/time-of-flight mass spectrometer (MALDI/TOF-MS), respectively.]. 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:NP483707.RANLTDxg_QWuWaOVa2ukl6tx9P2IvJA2ATEFFWp4nz3vk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:49+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" .
}