@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs> .
@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:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_head {
   this: np:hasAssertion dgn-np:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_assertion ;
    np:hasProvenance dgn-np:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_provenance ;
    np:hasPublicationInfo dgn-np:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_assertion a np:Assertion .
  dgn-np:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_provenance a np:Provenance .
  dgn-np:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_assertion {
   miriam-gene:2099 a ncit:C16612 .
  lld:C0007222 a ncit:C7057 .
  dgn-gda:DGN6591e1099c03e2a9ec07570be0d40616 sio:SIO_000628 miriam-gene:2099 , lld:C0007222 ;
    a sio:SIO_001122 .
}
dgn-np:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_provenance {
   dgn-np:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_assertion dcterms:description "[ Individuals with the common ESR1 c.454-397CC genotype have a substantial increase in risk of MI. Whether ESR1 c.454-397T>C is causally related to MI risk or in linkage disequilibrium with 1 or more causal variants remains to be determined. These findings support the importance of estrogen receptors in CVD susceptibility, especially in men. Estrogen receptor variation also has potential to explain recent conflicting data regarding the effects of hormone therapy on CVD susceptibility in women.]. 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:14600184 ;
    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:NP62584.RAsdwVj5C_9bGQbayGyt2glyLtK1TZUzdGB60TvsgsKqs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:29+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" .
}