@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ> .
@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:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_head {
  this: np:hasAssertion dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_assertion ;
    np:hasProvenance dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_assertion a np:Assertion .
  dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_provenance a np:Provenance .
  dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_assertion {
  miriam-gene:412 a ncit:C16612 .
  lld:C0020619 a ncit:C7057 .
  dgn-gda:DGNdcfc32bb414365836dd3af9eaed0500c sio:SIO_000628 miriam-gene:412 , lld:C0020619 ;
    a sio:SIO_001121 .
}
dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_provenance {
  dgn-np:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_assertion dcterms:description "[Flow cytometry and the use of special probes indicated that these two brothers had a large deletion of the short arm of the X chromosome which included the STS locus, the closely linked locus DXS237 and probably the gene for hypogonadism, findings which offer the opportunity for speculations on the locus of control of normal testicular development and function.]. 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:3150366 ;
    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:NP835456.RAxOni_ADLWSL81PNe43y8oeSyqSrAkAmyFAr5Bpl84jQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:31+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" .
}