@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8> .
@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:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_head {
  this: np:hasAssertion dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_assertion ;
    np:hasProvenance dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_provenance ;
    np:hasPublicationInfo dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_assertion a np:Assertion .
  dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_provenance a np:Provenance .
  dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_assertion {
  miriam-gene:4502 a ncit:C16612 .
  lld:C0011849 a ncit:C7057 .
  dgn-gda:DGN3dd3ba17af2cafaff4fcee8027a0dccf sio:SIO_000628 miriam-gene:4502 , lld:C0011849 ;
    a sio:SIO_001121 .
}
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_provenance {
  dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_assertion dcterms:description "[Using the PCR-based restriction fragment length polymorphism method, seven single nucleotide polymorphisms (SNPs) in MT genes (rs8052394 and rs11076161 in MT1A gene, rs8052334, rs964372, and rs7191779 in MT1B gene, rs708274 in MT1E gene, and rs10636 in MT2A gene) were detected in 851 Chinese people of Han descent (397 diabetes and 454 controls).]. 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:18349110 ;
    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:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:45+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" .
}