@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk> .
@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:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_head {
  this: np:hasAssertion dgn-np:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_assertion ;
    np:hasProvenance dgn-np:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_provenance ;
    np:hasPublicationInfo dgn-np:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_assertion a np:Assertion .
  dgn-np:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_provenance a np:Provenance .
  dgn-np:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_assertion {
  miriam-gene:79152 a ncit:C16612 .
  lld:C1853578 a ncit:C7057 .
  dgn-gda:DGNec8f99d8a145a0e357c3918114ee6aba sio:SIO_000628 miriam-gene:79152 , lld:C1853578 ;
    a sio:SIO_001121 .
}
dgn-np:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_provenance {
  dgn-np:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_assertion dcterms:description "[Neurodegeneration with brain iron accumulation (NBIA) involves several genetic disorders, two of which, aceruloplasminemia and neuroferritinopathy, are caused by mutations in genes directly involved in iron metabolic pathway, and others, such as pantothenate-kinase 2, phospholipase-A2 and fatty acid 2-hydroxylase associated neurodegeneration, are caused by mutations in genes coding for proteins involved in phospholipid metabolism.]. 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:22266337 ;
    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:NP736455.RANVeNTSK6TLOa0F3UL368fxXj191k559UnJ8hwzr52Jk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:27+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" .
}