@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak> .
@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:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_head {
  this: np:hasAssertion dgn-np:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_assertion;
    np:hasProvenance dgn-np:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_provenance;
    np:hasPublicationInfo dgn-np:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_assertion a np:Assertion .
  
  dgn-np:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_provenance a np:Provenance .
  
  dgn-np:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_assertion {
  miriam-gene:8431 a ncit:C16612 .
  
  lld:C0011847 a ncit:C7057 .
  
  dgn-gda:DGNb86e723a455b8fb21bc0f559612ec3b1 sio:SIO_000628 miriam-gene:8431, lld:C0011847;
    a sio:SIO_001121 .
}

dgn-np:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_provenance {
  dgn-np:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_assertion dcterms:description
      "[Interestingly, all of the subjects with the mutations were mildly or moderately obese at onset of diabetes, and analysis of the lineages of these individuals indicated that the SHP mutations were associated with obesity rather than with diabetes.]. 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:11136233;
    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:NP661319.RAXO1wGJM5D9qUmPY53IUBANpejd7e611NrXE7lC_i1ak130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}