@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA> .
@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:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_head {
  this: np:hasAssertion dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_assertion ;
    np:hasProvenance dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_provenance ;
    np:hasPublicationInfo dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_assertion a np:Assertion .
  dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_provenance a np:Provenance .
  dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_assertion {
  miriam-gene:6344 a ncit:C16612 .
  lld:C0031511 a ncit:C7057 .
  dgn-gda:DGNde5a189873dc75c96c54b8b3a872d39c sio:SIO_000628 miriam-gene:6344 , lld:C0031511 ;
    a sio:SIO_001121 .
}
dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_provenance {
  dgn-np:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_assertion dcterms:description "[We recently discovered that pheochromocytomas developing in rats affected by the MENX (multiple endocrine neoplasia-like) syndrome express at very high-level Sctr, encoding SR. We here report that SR are also highly abundant on the membranes of rat adrenal and extraadrenal pheochromocytoma, starting from early stages of tumor development, and are functional.]. 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:22692904 ;
    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:NP224060.RAde2YnWRiBM1EnYWidkhO7vaY1tf5wcEPF8sGt6H4fwA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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" .
}