@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s> .
@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:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_head {
  this: np:hasAssertion dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_assertion ;
    np:hasProvenance dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_provenance ;
    np:hasPublicationInfo dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_assertion a np:Assertion .
  dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_provenance a np:Provenance .
  dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_assertion {
  miriam-gene:7253 a ncit:C16612 .
  lld:C1262098 a ncit:C7057 .
  dgn-gda:DGN1c89e713e2c85c2e83a51494a545215b sio:SIO_000628 miriam-gene:7253 , lld:C1262098 ;
    a sio:SIO_001121 .
}
dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_provenance {
  dgn-np:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_assertion dcterms:description "[In order to compare the oncogenic potential of the activated mutant Gs alpha protein and the constitutively activated TSHR, we have transfected FRTL-5 cells with an expression vector bearing either the cDNA of the Gs alpha gene carrying the A201S mutation or the cDNA of the TSH receptor carrying the M453T mutation recently identified in a case of congenital hyperthyroidism.]. 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:9519872 ;
    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:NP635820.RA4F_1F-_l_tuHQw8uCBAaj4L9qHc2ZNrXBR-NLOyic-s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:23+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" .
}