@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_head {
   this: np:hasAssertion dgn-np:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_assertion ;
    np:hasProvenance dgn-np:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_provenance ;
    np:hasPublicationInfo dgn-np:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_assertion a np:Assertion .
  dgn-np:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_provenance a np:Provenance .
  dgn-np:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_assertion {
   miriam-gene:1080 a ncit:C16612 .
  lld:C0021364 a ncit:C7057 .
  dgn-gda:DGNf7cbccc18bade849524beb3566f9ec26 sio:SIO_000628 miriam-gene:1080 , lld:C0021364 ;
    a sio:SIO_001121 .
}
dgn-np:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_provenance {
   dgn-np:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_assertion dcterms:description "[Thus in a very near future, for a comprehensive male infertility panel, it will be essential to include additional genetic tests, such as CFTR gene mutations, sperm mitochondrial DNA mutations, and androgen receptor gene mutations, besides the conventional chromosomal analyses, Y chromosome microdeletion detection, and sperm-FISH analyses.]. 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:18554162 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP676662.RAbOFRDJ_dzBBY5x9Dtmpmd_OLEpYjDCFSc6TLb7jiqL0130_publicationInfo {
   this: dcterms:created "2016-05-13T12:46:52+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}