@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y> .
@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:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_head {
  this: np:hasAssertion dgn-np:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_assertion ;
    np:hasProvenance dgn-np:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_provenance ;
    np:hasPublicationInfo dgn-np:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_assertion a np:Assertion .
  dgn-np:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_provenance a np:Provenance .
  dgn-np:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_assertion {
  miriam-gene:6473 a ncit:C16612 .
  lld:C0013336 a ncit:C7057 .
  dgn-gda:DGN9057f887cfa491952c65099cd3c592fc sio:SIO_000628 miriam-gene:6473 , lld:C0013336 ;
    a sio:SIO_001121 .
}
dgn-np:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_provenance {
  dgn-np:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_assertion dcterms:description "[Our results imply that deletion carriers have no augmented risk of SHOX-related pathologies (short stature and skeletal anomalies) and indicate that there is no need for radical changes in genetic counseling of Yq microdeletion carriers attempting ART, since the only risk established so far for their male offspring remains impaired spermatogenesis.]. 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:24008148 ;
    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:NP1107851.RABz_UegnMkbHk6rd0HW3oJza7vIY7ZeKnYnoGnLVig0Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:08+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" .
}