@prefix dct: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg> .
@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 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:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_head {
  this: np:hasAssertion dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_assertion ;
    np:hasProvenance dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_provenance ;
    np:hasPublicationInfo dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_assertion a np:Assertion .
  dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_provenance a np:Provenance .
  dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_assertion {
  miriam-gene:23560 a ncit:C16612 .
  lld:C0040136 a ncit:C7057 .
  dgn-gda:DGNd7a9b6c872ace969121d6cb888455599 sio:SIO_000628 miriam-gene:23560 , lld:C0040136 ;
    a sio:SIO_001121 .
}
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_provenance {
  dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_assertion dct:description "[The postulated proto-oncogenic character of the gene encoding the alpha sub-unit of the stimulatory GTP-binding protein Gs alpha (gsp) in pituitary and thyroid tumors, the finding of identical somatic gsp mutations in the myocardium of patients with McCune-Albright syndrome, and the associated endocrine anomalies of the Carney complex prompted us to investigate the occurrence of activating missense mutations in the Gs alpha gene in 10 sporadically occurring atrial myxomas and in 8 tumors from 7 patients with Carney complex.]. 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:8698339 ;
    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:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_publicationInfo {
  this: dct:created "2014-10-02T12:41:34+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct: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" .
}