@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ> .
@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:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_head {
  this: np:hasAssertion dgn-np:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_assertion ;
    np:hasProvenance dgn-np:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_assertion a np:Assertion .
  dgn-np:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_provenance a np:Provenance .
  dgn-np:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_assertion {
  miriam-gene:2966 a ncit:C16612 .
  lld:C0026847 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_provenance {
  dgn-np:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_assertion dcterms:description "[The spinal muscular atrophy candidate interval genes including survival motor neuron, the responsible gene in spinal muscular atrophy phenotype expression, neuronal apoptosis inhibitory protein, and P44, potential modifying genes, are located on chromosome 5q13 in two highly homologous copies (telomeric and centromeric) within the spinal muscular atrophy region.]. 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:17903057 ;
    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:NP636921.RADRX-ef9utfsUrOBW3xUPVxtNNAMmiqnWV6FWrUmPqAQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:24+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> ;
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    pav:version "v2.1.0.0" .
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}