@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM> .
@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:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_head {
  this: np:hasAssertion dgn-np:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_assertion ;
    np:hasProvenance dgn-np:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_provenance ;
    np:hasPublicationInfo dgn-np:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_assertion a np:Assertion .
  dgn-np:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_provenance a np:Provenance .
  dgn-np:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_assertion {
  miriam-gene:1437 a ncit:C16612 .
  lld:C0152025 a ncit:C7057 .
  dgn-gda:DGNd80c88e654c7f1a35027ad7aa63027c4 sio:SIO_000628 miriam-gene:1437 , lld:C0152025 ;
    a sio:SIO_001121 .
}
dgn-np:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_provenance {
  dgn-np:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_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:NP448633.RABIPtDYCfJ63Q7-8_mmlwckF9yHNj3QQ5cLjLWK6gCMM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:27+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> ;
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}