@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk> .
@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:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_head {
  this: np:hasAssertion dgn-np:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_assertion ;
    np:hasProvenance dgn-np:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_provenance ;
    np:hasPublicationInfo dgn-np:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_assertion a np:Assertion .
  dgn-np:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_provenance a np:Provenance .
  dgn-np:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_assertion {
  miriam-gene:6638 a ncit:C16612 .
  lld:C0021359 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_provenance {
  dgn-np:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_assertion dcterms:description "[To test this hypothesis, we have studied the methylation levels of 2 paternally (H19 and GTL2) and 5 maternally methylated (LIT1, MEST, NESPAS, PEG3, and SNRPN) imprinted genes, as well as of ALU and LINE1 repetitive elements in 141 sperm samples, which were used for assisted reproductive technologies (ART), including 106 couples with strictly male-factor or combined male and female infertility and 28 couples with strictly female-factor infertility.]. 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 ;
    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:NP673871.RAIEGlpjpSU6zehDVphogiL_wtSkmMtR34kTa0er6deFk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:47+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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