@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM> .
@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:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_head {
  this: np:hasAssertion dgn-np:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_assertion ;
    np:hasProvenance dgn-np:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_provenance ;
    np:hasPublicationInfo dgn-np:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_assertion a np:Assertion .
  dgn-np:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_provenance a np:Provenance .
  dgn-np:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_assertion {
  miriam-gene:2706 a ncit:C16612 .
  lld:C0238286 a ncit:C7057 .
  dgn-gda:DGNadd6843cfe22ebd68ff23760c4d180ec sio:SIO_000628 miriam-gene:2706 , lld:C0238286 ;
    a sio:SIO_001121 .
}
dgn-np:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_provenance {
  dgn-np:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_assertion dcterms:description "[The tests included two diseases associated with death in childhood (Niemann-Pick type A and Tay-Sachs disease), five with moderate disability and a variably shortened life span (Bloom syndrome, Canavan disease, cystic fibrosis, familial dysautonomia, Fanconi anemia, and mucolipidosis type IV), and two diseases that are not necessarily disabling or routinely shorten the lifespan (Gaucher disease type I and DFNB1 sensorineural hearing loss).]. 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:15775754 ;
    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:NP414808.RA88t3tnuHW-OMh_xLLD0qUSZGJG4wrQHav2prKxrnYFM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:06+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" .
}