@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM> .
@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:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_head {
  this: np:hasAssertion dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_assertion;
    np:hasProvenance dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_provenance;
    np:hasPublicationInfo dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_assertion a np:Assertion .
  
  dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_provenance a np:Provenance .
  
  dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_assertion {
  miriam-gene:3480 a ncit:C16612 .
  
  lld:C0010278 a ncit:C7057 .
  
  dgn-gda:DGNe8b4e9976491f785c335ba5bcb61d22c sio:SIO_000628 miriam-gene:3480, lld:C0010278;
    a sio:SIO_001121 .
}

dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_provenance {
  dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_assertion dcterms:description
      "[Taken together, these results suggest that despite the stimulation of different pathways, activating phosphorylation patterns for IRS1 were consistent in cell lines from both subtypes and the IGF1R variants, thus implicating a key role for IRS1 in the pathogenesis of nonsyndromic craniosynostosis.]. 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:23073384;
    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:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:10+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" .
}