@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4> .
@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:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_head {
   this: np:hasAssertion dgn-np:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_assertion ;
    np:hasProvenance dgn-np:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_provenance ;
    np:hasPublicationInfo dgn-np:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_assertion a np:Assertion .
  dgn-np:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_provenance a np:Provenance .
  dgn-np:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_assertion {
   miriam-gene:4524 a ncit:C16612 .
  lld:C0279628 a ncit:C7057 .
  dgn-gda:DGNd3f9dc433f9d6a331fa284d9b33de1f3 sio:SIO_000628 miriam-gene:4524 , lld:C0279628 ;
    a sio:SIO_001121 .
}
dgn-np:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_provenance {
   dgn-np:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_assertion dcterms:description "[In this study, we evaluated MTHFR C677T and A1298C polymorphisms, and vitamin B12, folate, and plasma homocystein levels in patients with esophageal adenocarcinoma (EAC), Barrett's esophagus (BE), chronic esophagitis, and healthy controls (n = 26, n = 14, n = 30, and n = 30, respectively).]. 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:21951971 ;
    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:NP699492.RAAWSps0qEcebkpOhKi-hBZWUgs3aykIcDm9H8CGsouB4130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:05+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" .
}