@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP297982.RA0ou7YO9OqEV7wCaFOIsISJVBncoL-HDK-KIMomY_MJ4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP297982.RA0ou7YO9OqEV7wCaFOIsISJVBncoL-HDK-KIMomY_MJ4130_head {
  this: np:hasAssertion dgn-np:NP297982.RA0ou7YO9OqEV7wCaFOIsISJVBncoL-HDK-KIMomY_MJ4130_assertion;
    np:hasProvenance dgn-np:NP297982.RA0ou7YO9OqEV7wCaFOIsISJVBncoL-HDK-KIMomY_MJ4130_provenance;
    np:hasPublicationInfo dgn-np:NP297982.RA0ou7YO9OqEV7wCaFOIsISJVBncoL-HDK-KIMomY_MJ4130_publicationInfo;
    a np:Nanopublication .
  
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      np:PublicationInfo .
}

dgn-np:NP297982.RA0ou7YO9OqEV7wCaFOIsISJVBncoL-HDK-KIMomY_MJ4130_assertion {
  miriam-gene:5291 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP297982.RA0ou7YO9OqEV7wCaFOIsISJVBncoL-HDK-KIMomY_MJ4130_provenance {
  dgn-np:NP297982.RA0ou7YO9OqEV7wCaFOIsISJVBncoL-HDK-KIMomY_MJ4130_assertion dcterms:description
      "[Our results show that (1) the TSHR(M623) or (M632) cDNAs give rise to 3T3 clones presenting a fully neoplastic phenotype (growth in agar and nude mouse tumorigenesis); this phenotype was weaker in the cells transformed by the 632 cDNA; (2) suggest that the fully transformed phenotype of our 3T3 cells, may be the consequence of the additive effect of the activation of at least two different pathways: the cAMP pathway through G(alpha)s and the Ras dependent MAPK pathway through G(beta)gamma and PI3K and (3) show that the PI3K isoform playing a key role as an effector in the MAPK pathway activation in our 3T3-transformed cells is PI3Kgamma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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  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:NP297982.RA0ou7YO9OqEV7wCaFOIsISJVBncoL-HDK-KIMomY_MJ4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:00+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
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