@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI> .
@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:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_head {
  this: np:hasAssertion dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_assertion;
    np:hasProvenance dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_provenance;
    np:hasPublicationInfo dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_assertion a np:Assertion .
  
  dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_provenance a np:Provenance .
  
  dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_assertion {
  miriam-gene:2778 a ncit:C16612 .
  
  lld:C0040136 a ncit:C7057 .
  
  dgn-gda:DGN795baba59a44dcc3bfd8bd754b5184d0 sio:SIO_000628 miriam-gene:2778, lld:C0040136;
    a sio:SIO_001121 .
}

dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_provenance {
  dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_assertion dcterms:description
      "[Acquisition of a similar activating mutation in GNAS1 later in life presumably accounts for the restricted distribution of the gsp oncogene, and is associated with the development of isolated lesions (for example, fibrous dysplasia, pituitary or thyroid tumors) without other manifestations of MAS.]. 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:8699958;
    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:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:37+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" .
}