@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc> .
@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:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_head {
  this: np:hasAssertion dgn-np:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_assertion;
    np:hasProvenance dgn-np:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_provenance;
    np:hasPublicationInfo dgn-np:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_assertion a np:Assertion .
  
  dgn-np:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_provenance a np:Provenance .
  
  dgn-np:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_assertion {
  miriam-gene:5291 a ncit:C16612 .
  
  lld:C1520166 a ncit:C7057 .
  
  dgn-gda:DGNf2f47f4043ee73c23a6efa560e3111be sio:SIO_000628 miriam-gene:5291, lld:C1520166;
    a sio:SIO_001121 .
}

dgn-np:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_provenance {
  dgn-np:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_assertion dcterms:description
      "[Specifically, introduction of a subset of the mutations identified in human GBM, in the nSH2 and iSH2 domains, increases signaling through the PI3K pathway and promotes tumorigenesis of primary normal human astrocytes in an orthotopic xenograft model.]. 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:23166678;
    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:NP317945.RAT3YmuRa6cKVc1LMemSQgAsxBw3UgCJ9HSNo_kTwaMlc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:04+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" .
}