@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ> .
@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:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_head {
  this: np:hasAssertion dgn-np:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_assertion;
    np:hasProvenance dgn-np:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_provenance;
    np:hasPublicationInfo dgn-np:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_assertion a np:Assertion .
  
  dgn-np:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_provenance a np:Provenance .
  
  dgn-np:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_assertion {
  miriam-gene:2778 a ncit:C16612 .
  
  lld:C0242292 a ncit:C7057 .
  
  dgn-gda:DGNaa48ff75c104fd2c22d237c6372513bb sio:SIO_000628 miriam-gene:2778, lld:C0242292;
    a sio:SIO_001121 .
}

dgn-np:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_provenance {
  dgn-np:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_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:NP262523.RAVbygOYDok58WN3wDIfj9DlXwWxHliO1W_qE7y_8mUkQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}