@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc> .
@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:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_head {
  this: np:hasAssertion dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_assertion ;
    np:hasProvenance dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_provenance ;
    np:hasPublicationInfo dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_assertion a np:Assertion .
  dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_provenance a np:Provenance .
  dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_assertion {
  miriam-gene:2253 a ncit:C16612 .
  lld:C0206718 a ncit:C7057 .
  dgn-gda:DGNd816489f97b3046155c9c1a35ad337d9 sio:SIO_000628 miriam-gene:2253 , lld:C0206718 ;
    a sio:SIO_001121 .
}
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_provenance {
  dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_assertion dcterms:description "[In accordance with these in vitro findings, the immunohistochemical analysis on human neurological diseases showed that FGF8 expression is evident in differentiating histological types of neuroblastoma and ganglioneuroblastoma, and that the levels of FGF8 immunoreactivity in the substantia nigra from Parkinson's disease are significantly lower than those in age-matched controls.]. 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:11532426 ;
    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:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:42+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" .
}