@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8> .
@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:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_head {
  this: np:hasAssertion dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_assertion ;
    np:hasProvenance dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_provenance ;
    np:hasPublicationInfo dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_assertion a np:Assertion .
  dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_provenance a np:Provenance .
  dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_assertion {
  miriam-gene:383 a ncit:C16612 .
  lld:C0026838 a ncit:C7057 .
  dgn-gda:DGN590d81a86944237aea314ae9edf39ecf sio:SIO_000628 miriam-gene:383 , lld:C0026838 ;
    a sio:SIO_001121 .
}
dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_provenance {
  dgn-np:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_assertion dcterms:description "[Since the spasticity and paucity of hyperammonemic crises seen in human AI-deficient patients are not features of the other urea cycle disorders, the likelihood of ammonia as the main neuropathogenic agent becomes extremely low, and the modest elevations of arginine seen in the brains of our mouse model of hyperargininemia make it an unlikely candidate as well.]. 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:17997338 ;
    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:NP698931.RAYK2SRhxjJDL_PuMgDaDyEZ-Y46QalkCzSvYYJj-_Em8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:05+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" .
}