@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac> .
@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:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_head {
  this: np:hasAssertion dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_assertion ;
    np:hasProvenance dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_provenance ;
    np:hasPublicationInfo dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_assertion a np:Assertion .
  dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_provenance a np:Provenance .
  dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_assertion {
  miriam-gene:346673 a ncit:C16612 .
  lld:C0028960 a ncit:C7057 .
  dgn-gda:DGN08f5abdd435a93cf3d00dcc94b5a0d1d sio:SIO_000628 miriam-gene:346673 , lld:C0028960 ;
    a sio:SIO_001121 .
}
dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_provenance {
  dgn-np:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_assertion dcterms:description "[The genetic variant rs10269148 of STRA8 gene showed higher risk of spermatogenic impairment in the groups of abnormospermia (including azoospermia subgroup and oligozoospermia subgroup) and azoospermia than the controls with odds ratios and 95% confidence intervals of 2.52 (1.29-4.94) and 2.92 (1.41-6.06), respectively (Pā€Š=ā€Š0.006, 0.002 respective).]. 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:23320086 ;
    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:NP694295.RAPd6GXwPgOs6siyQHPZsUMnOTAwNVyg8jnh9-5FEW_Ac130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:02+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> ;
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}