@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk> .
@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:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_head {
   this: np:hasAssertion dgn-np:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_assertion ;
    np:hasProvenance dgn-np:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_provenance ;
    np:hasPublicationInfo dgn-np:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_assertion a np:Assertion .
  dgn-np:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_provenance a np:Provenance .
  dgn-np:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_assertion {
   miriam-gene:6611 a ncit:C16612 .
  lld:C0026351 a ncit:C7057 .
  dgn-gda:DGNcb36efab72b858378a7e2c6c8b6f8af6 sio:SIO_000628 miriam-gene:6611 , lld:C0026351 ;
    a sio:SIO_001121 .
}
dgn-np:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_provenance {
   dgn-np:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_assertion dcterms:description "[The affected males have mild-to-moderate mental retardation (MR), hypotonia, cerebellar circuitry dysfunction, facial asymmetry, thin habitus, osteoporosis, kyphoscoliosis, decreased activity of SMS, correspondingly low levels of intracellular spermine in lymphocytes and fibroblasts, and elevated spermidine/spermine ratios.]. 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:14508504 ;
    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:NP875332.RAZUhWePoeRSS_yxqpbfAXIzAEsj2RbbhX2a0gpFWuOpk130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:55+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" .
}