@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI> .
@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:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_head {
  this: np:hasAssertion dgn-np:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_assertion;
    np:hasProvenance dgn-np:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_provenance;
    np:hasPublicationInfo dgn-np:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_assertion a np:Assertion .
  
  dgn-np:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_provenance a np:Provenance .
  
  dgn-np:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGN0aa9adfe50cb94870a87314a0429eed0 sio:SIO_000628 miriam-gene:3630, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_provenance {
  dgn-np:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_assertion dcterms:description
      "[We conclude that severity of insulin resistance in the proband may be explained by the genetic condition of compound heterozygote for IR mutations while severe insulin resistance in the mother raises the possibility that other genetic factors, like IRS-1 polymorphisms, may contribute to the phenotypic expression of IR mutations.]. 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:9175790;
    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:NP503121.RATvwke5qqOZRv9q0Intwj2CrXM-AwdLVgTPFGA8Jf2ZI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:00+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" .
}