@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0> .
@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:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_head {
   this: np:hasAssertion dgn-np:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_assertion ;
    np:hasProvenance dgn-np:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_provenance ;
    np:hasPublicationInfo dgn-np:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_assertion a np:Assertion .
  dgn-np:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_provenance a np:Provenance .
  dgn-np:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_assertion {
   miriam-gene:3481 a ncit:C16612 .
  lld:C0021364 a ncit:C7057 .
  dgn-gda:DGNca36d87d4b56c7ffdd735f688f7f18db sio:SIO_000628 miriam-gene:3481 , lld:C0021364 ;
    a sio:SIO_001121 .
}
dgn-np:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_provenance {
   dgn-np:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_assertion dcterms:description "[Epimutations (often hypermethylation) in several genes, namely MTHFR, PAX8, NTF3, SFN, HRAS, JHM2DA, IGF2, H19, RASGRF1, GTL2, PLAG1, D1RAS3, MEST, KCNQ1, LIT1, and SNRPN, have been reported in association with poor semen parameters or male infertility.]. 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:21540125 ;
    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:NP479658.RA3ngr-Wz1X7lEV2ncIcFQZNWhDKVFALH-fEX3ikNDMQ0130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:47+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" .
}