@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g> .
@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:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_head {
  this: np:hasAssertion dgn-np:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_assertion ;
    np:hasProvenance dgn-np:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_provenance ;
    np:hasPublicationInfo dgn-np:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_assertion a np:Assertion .
  dgn-np:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_provenance a np:Provenance .
  dgn-np:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_assertion {
  miriam-gene:5322 a ncit:C16612 .
  lld:C0524851 a ncit:C7057 .
  dgn-gda:DGNa3281c9e40f5628c54886092391a355f sio:SIO_000628 miriam-gene:5322 , lld:C0524851 ;
    a sio:SIO_001121 .
}
dgn-np:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_provenance {
  dgn-np:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_assertion dcterms:description "[In contrast, no loss of function or common (minor-allele frequency>0.05%) nonsynonymous PLA2G5 variants have been previously reported (EVS, dbSNP, 1000 Genomes Project) or were detected in an internal database of 224 exomes (from subjects with adult onset neurodegenerative disease and without a diagnosis of ophthalmic disease).]. 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:22137173 ;
    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:NP326246.RA4aVIhpUoPLhp-1u1kCYetLMJSjFEDYuRL0AQiIswH4g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:10+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" .
}