@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE> .
@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#> .
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  this: np:hasAssertion dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_assertion ;
    np:hasProvenance dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_provenance ;
    np:hasPublicationInfo dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_assertion a np:Assertion .
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  dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_assertion {
  miriam-gene:5295 a ncit:C16612 .
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dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_provenance {
  dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_assertion dcterms:description "[Our findings extend the genetic causes of severe insulin-resistance syndromes and provide important information with respect to the function of PIK3R1 in normal development and its role in human diseases, including growth delay, Rieger anomaly and other ocular affections, insulin resistance, diabetes, paucity of fat, and ovarian cysts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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dgn-np:NP474188.RAxNzGKpiWpJMfP4wVLGeOtiaa9w3sMNLtHyIVLGHNEFE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:44+02:00"^^xsd:dateTime ;
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