@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_head {
   this: np:hasAssertion dgn-np:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_assertion ;
    np:hasProvenance dgn-np:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_provenance ;
    np:hasPublicationInfo dgn-np:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_assertion a np:Assertion .
  dgn-np:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_provenance a np:Provenance .
  dgn-np:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_assertion {
   miriam-gene:2175 a ncit:C16612 .
  lld:C0015625 a ncit:C7057 .
  dgn-gda:DGNe9644d79282fc12af6ae49fa1696e404 sio:SIO_000628 miriam-gene:2175 , lld:C0015625 ;
    a sio:SIO_001121 .
}
dgn-np:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_provenance {
   dgn-np:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_assertion dcterms:description "[Mutations in 16 genes (FANCA, B, C, D1, D2, E, F, G, I, J, L, M, N, O, P, and Q) have been identified in patients, with the Fanconi anemia subtype J (FA-J) resulting from homozygous mutations in the FANCJ gene.]. 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:25070891 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP393429.RApl_Cg-ZEN50UlpTKyIHpwdZMQf6EAL8u_Qw1tVl4bW4130_publicationInfo {
   this: dcterms:created "2015-08-25T14:41:28+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}