@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM> .
@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:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_head {
  this: np:hasAssertion dgn-np:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_assertion ;
    np:hasProvenance dgn-np:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_provenance ;
    np:hasPublicationInfo dgn-np:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_assertion a np:Assertion .
  dgn-np:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_provenance a np:Provenance .
  dgn-np:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_assertion {
  miriam-gene:7276 a ncit:C16612 .
  lld:C0007194 a ncit:C7057 .
  dgn-gda:DGN93c5dc6a966fb7132a2c9008a52ac249 sio:SIO_000628 miriam-gene:7276 , lld:C0007194 ;
    a sio:SIO_001121 .
}
dgn-np:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_provenance {
  dgn-np:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_assertion dcterms:description "[We assessed the phenotypic and genotypic spectra of ATTR in a Caucasian area and evaluated the prevalence, genetic background, and disease profile of cases with an exclusively cardiac phenotype, highlighting possible hints for the differential diagnosis with hypertrophic cardiomyopathy (HCM) and senile systemic amyloidosis (SSA).]. 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:22745357 ;
    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:NP275079.RA17x5dOa8fkIb-dBnJfl0j1uWmktXsldYzITlLUdU3pM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:35+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" .
}