@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o> .
@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:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_head {
  this: np:hasAssertion dgn-np:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_assertion ;
    np:hasProvenance dgn-np:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_provenance ;
    np:hasPublicationInfo dgn-np:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_assertion a np:Assertion .
  dgn-np:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_provenance a np:Provenance .
  dgn-np:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_assertion {
  miriam-gene:8674 a ncit:C16612 .
  lld:C0011860 a ncit:C7057 .
  dgn-gda:DGN38b5fda4b97fc9a2b2e5b838329a64fb sio:SIO_000628 miriam-gene:8674 , lld:C0011860 ;
    a sio:SIO_001121 .
}
dgn-np:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_provenance {
  dgn-np:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_assertion dcterms:description "[Polymorphisms in and around VAMP4 were genotyped in 65 Amish subjects with T2DM, 64 subjects with impaired glucose homeostasis (IGH), and 126 normal glucose tolerant controls, as well as in an expanded set of 749 participants of the Amish Family Diabetes Study for whom glucose and insulin levels during an oral glucose tolerance test (OGTT) and other quantitative traits related to diabetes were available.]. 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:15896658 ;
    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:NP510013.RAYzmeC09SBP0YvS5k1446vtiRLPNqcT4JPCa1ltHgX9o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:04+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" .
}