@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP399346.RABo8WX7bybxOHPtwrHGg1IpON1_EzCmlY6g-QDc1AEVA> .
@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:NP399346.RABo8WX7bybxOHPtwrHGg1IpON1_EzCmlY6g-QDc1AEVA130_head {
  this: np:hasAssertion dgn-np:NP399346.RABo8WX7bybxOHPtwrHGg1IpON1_EzCmlY6g-QDc1AEVA130_assertion ;
    np:hasProvenance dgn-np:NP399346.RABo8WX7bybxOHPtwrHGg1IpON1_EzCmlY6g-QDc1AEVA130_provenance ;
    np:hasPublicationInfo dgn-np:NP399346.RABo8WX7bybxOHPtwrHGg1IpON1_EzCmlY6g-QDc1AEVA130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP399346.RABo8WX7bybxOHPtwrHGg1IpON1_EzCmlY6g-QDc1AEVA130_provenance a np:Provenance .
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}
dgn-np:NP399346.RABo8WX7bybxOHPtwrHGg1IpON1_EzCmlY6g-QDc1AEVA130_assertion {
  miriam-gene:2693 a ncit:C16612 .
  lld:C0149721 a ncit:C7057 .
  dgn-gda:DGNe3e56fbadc39f27d6c121877ff017fbd sio:SIO_000628 miriam-gene:2693 , lld:C0149721 ;
    a sio:SIO_001121 .
}
dgn-np:NP399346.RABo8WX7bybxOHPtwrHGg1IpON1_EzCmlY6g-QDc1AEVA130_provenance {
  dgn-np:NP399346.RABo8WX7bybxOHPtwrHGg1IpON1_EzCmlY6g-QDc1AEVA130_assertion dcterms:description "[We performed a comprehensive analysis of SNPs, linkage disequilibrium (LD), and haplotype structure across the entire GHSR gene region (99.3 kb) in 178 pedigrees with multiple obese members (DNA of 1,095 Caucasians) and in an independent sample of the general population (MONICA Augsburg left ventricular hypertrophy substudy; DNA of 1,418 Caucasians).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP399346.RABo8WX7bybxOHPtwrHGg1IpON1_EzCmlY6g-QDc1AEVA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:58+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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    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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