@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_head {
   this: np:hasAssertion dgn-np:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_assertion ;
    np:hasProvenance dgn-np:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_provenance ;
    np:hasPublicationInfo dgn-np:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_assertion a np:Assertion .
  dgn-np:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_provenance a np:Provenance .
  dgn-np:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_assertion {
   miriam-gene:4221 a ncit:C16612 .
  lld:C0567439 a ncit:C7057 .
  dgn-gda:DGNacd28643dcd2c7cb0d802f2ef31e8ea9 sio:SIO_000628 miriam-gene:4221 , lld:C0567439 ;
    a sio:SIO_001121 .
}
dgn-np:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_provenance {
   dgn-np:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_assertion dcterms:description "[Similarly, there is little evidence to suggest that the mutations involved in genetic syndromes associated with pituitary tumors (such as the gsp, MEN1, PKAR1A or AIP mutations) are common in sporadic tumors.]. 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:19058014 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP553598.RA-yBphCD5m4N3cUKb2aOblXyJ4S2YkCR8omgtxjXYVeE130_publicationInfo {
   this: dcterms:created "2015-08-25T14:43:07+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}