@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c> .
@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:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_head {
  this: np:hasAssertion dgn-np:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_assertion ;
    np:hasProvenance dgn-np:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_provenance ;
    np:hasPublicationInfo dgn-np:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_assertion a np:Assertion .
  dgn-np:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_provenance a np:Provenance .
  dgn-np:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_assertion {
  miriam-gene:51738 a ncit:C16612 .
  lld:C0010068 a ncit:C7057 .
  dgn-gda:DGN2836f9db443754f22721f2eb6f9272f3 sio:SIO_000628 miriam-gene:51738 , lld:C0010068 ;
    a sio:SIO_001121 .
}
dgn-np:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_provenance {
  dgn-np:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_assertion dcterms:description "[Seven single nucleotide polymorphisms (SNPs) covering the GHSR region as well as eight SNPs across the ghrelin gene (GHRL) region were genotyped in index MI patients (864 Caucasians, 'index MI cases') from the German MI family study and in matched controls without evidence of CAD (864 Caucasians, 'controls', MONICA Augsburg).]. 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:17324965 ;
    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:NP329679.RA7iQmotUm1XbLQJna4wsLzpG3rHGG7SmfWZC99ME_w3c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:14+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" .
}