@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg> .
@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:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_head {
  this: np:hasAssertion dgn-np:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_assertion ;
    np:hasProvenance dgn-np:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_provenance ;
    np:hasPublicationInfo dgn-np:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_assertion a np:Assertion .
  dgn-np:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_provenance a np:Provenance .
  dgn-np:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_assertion {
  miriam-gene:84691 a ncit:C16612 .
  lld:C0028754 a ncit:C7057 .
  dgn-gda:DGN9f09f4c7dc239ca9f99a0a2bfd6f6e4b sio:SIO_000628 miriam-gene:84691 , lld:C0028754 ;
    a sio:SIO_001122 .
}
dgn-np:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_provenance {
  dgn-np:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_assertion dcterms:description "[Using a P-value of 0.01 as criteria for association in the linked families, a P-value of 0.05 as criteria for association in the unrelated sample, and requiring consistency in the direction of the effect of the minor allele between the two samples, we identified two coding SNPs in the NYD-SP18 gene with minor alleles increasing the risk of obesity.]. 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:18317470 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP85931.RALuY43YSp-BuPiUkn9YYpw8_w8fCZAB2GOWiMaXkUljg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+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> ;
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}