@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs> .
@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:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_head {
  this: np:hasAssertion dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_assertion;
    np:hasProvenance dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_provenance;
    np:hasPublicationInfo dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_assertion a np:Assertion .
  
  dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_provenance a np:Provenance .
  
  dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_assertion {
  miriam-gene:3667 a ncit:C16612 .
  
  lld:C0021655 a ncit:C7057 .
  
  dgn-gda:DGNd5943b2790dd91d7a362b4226e10db47 sio:SIO_000628 miriam-gene:3667, lld:C0021655;
    a sio:SIO_001122 .
}

dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_provenance {
  dgn-np:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_assertion dcterms:description
      "[ While subtle effects of these variants cannot be excluded in this system, it is unlikely that these variants are responsible for the extreme insulin resistance seen in the subjects harbouring them. Although IRS proteins play a central role in insulin signalling, functionally significant mutations in the IRS-1 gene are a rare cause of human syndromes of severe insulin resistance.]. 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:12358865;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP55817.RAhg6IK5C1rV7fLJUcQbX1HwT9ZovdgOwHDe0rnacwdbs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}