@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM> .
@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:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_head {
  this: np:hasAssertion dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_assertion;
    np:hasProvenance dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_provenance;
    np:hasPublicationInfo dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_assertion a np:Assertion .
  
  dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_provenance a np:Provenance .
  
  dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_assertion {
  miriam-gene:50511 a ncit:C16612 .
  
  lld:C1847540 a ncit:C7057 .
  
  dgn-gda:DGN799ea9cd691c8bb3014ff046523d4942 sio:SIO_000628 miriam-gene:50511, lld:C1847540;
    a sio:SIO_001121 .
}

dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_provenance {
  dgn-np:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_assertion dcterms:description
      "[On the basis of the results, we agree with the idea that SYCP3 mutations are not associated with the genetic susceptibility for meiotic arrest in infertile male patients with nonobstructive azoospermia in the Turkish population and that further studies investigating the other components of the synaptonemal complex protein (SYCP1, SYCP2) should be conducted.]. 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:22670862;
    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:NP909613.RAiHIUY-hHIs-RDRP38ew6Oza8r-BPSdEqoe2G8-xgjRM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:18+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" .
}