@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU> .
@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:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_head {
  this: np:hasAssertion dgn-np:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_assertion;
    np:hasProvenance dgn-np:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_provenance;
    np:hasPublicationInfo dgn-np:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_assertion a np:Assertion .
  
  dgn-np:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_provenance a np:Provenance .
  
  dgn-np:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_assertion {
  miriam-gene:3052 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN00ca1d6dc28c35d539a5caea9ffde676 sio:SIO_000628 miriam-gene:3052, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_provenance {
  dgn-np:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_assertion dcterms:description
      "[Using affected sib pair methods (two-point linkage and multipoint linkage analyses), significant results were obtained with the 20q13 region, in the vicinity of the PCK1 locus, only in the subset of 55 early onset NIDDM sib pairs (multipoint MLS = 2.74, P = 0.0004; MLS = 2.34, P = 0.0009 when using a conservative weighting procedure).]. 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:9285775;
    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:NP733062.RAcT5XrzWQqokEbUeuSEwhc09Ji4tyArAUNuO1o12kMCU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:24+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" .
}