@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY> .
@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:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_head {
  this: np:hasAssertion dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_assertion ;
    np:hasProvenance dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_provenance ;
    np:hasPublicationInfo dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_assertion a np:Assertion .
  dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_provenance a np:Provenance .
  dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_assertion {
  miriam-gene:158 a ncit:C16612 .
  lld:C0268126 a ncit:C7057 .
  dgn-gda:DGN2b794d6cb547c7682d1fa3a246681b54 sio:SIO_000628 miriam-gene:158 , lld:C0268126 ;
    a sio:SIO_001121 .
}
dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_provenance {
  dgn-np:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_assertion dcterms:description "[The results also corroborate the hypothesis that the phenotypic severity of ADSL deficiency is mainly determined by structural stability and residual catalytic capacity of the corresponding mutant ADSL protein complexes, as this is prerequisite for the formation and stability of the purinosome and at least partial channeling of succinylaminoimidazolecarboxamide riboside-ADSL enzyme substrates-through the DNPS pathway.]. 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:22180458 ;
    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:NP687880.RAhnbQACRe4-n6a4DLzA-lNtuGWBmBU4_U-1m24zJByEY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:58+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" .
}