@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8> .
@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:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_head {
  this: np:hasAssertion dgn-np:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_assertion ;
    np:hasProvenance dgn-np:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_provenance ;
    np:hasPublicationInfo dgn-np:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_assertion a np:Assertion .
  dgn-np:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_provenance a np:Provenance .
  dgn-np:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_assertion {
  miriam-gene:8843 a ncit:C16612 .
  lld:C0406810 a ncit:C7057 .
  dgn-gda:DGN0c39f769f85b16ceef17abb6f182721a sio:SIO_000628 miriam-gene:8843 , lld:C0406810 ;
    a sio:SIO_001121 .
}
dgn-np:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_provenance {
  dgn-np:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_assertion dcterms: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:NP493993.RA0Yizj2ElEo5QgrvidL1atHTVoN5BYZE22PCZE063_t8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:55+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" .
}