@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_head { this: np:hasAssertion dgn-np:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_assertion; np:hasProvenance dgn-np:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_provenance; np:hasPublicationInfo dgn-np:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_publicationInfo; a np:Nanopublication . dgn-np:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_assertion a np:Assertion . dgn-np:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_provenance a np:Provenance . dgn-np:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_publicationInfo a np:PublicationInfo . } dgn-np:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_assertion { miriam-gene:6736 a ncit:C16612 . lld:C0432470 a ncit:C7057 . dgn-gda:DGN4cbf47f2402e994d51123c829d0305b2 sio:SIO_000628 miriam-gene:6736, lld:C0432470; a sio:SIO_001121 . } dgn-np:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_provenance { dgn-np:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_assertion dcterms:description "[On the assumption that the function of the testis is to produce hormones and spermatozoa, the hypothesis of a single Y-chromosomal testis-determining gene with a dominant effect is shown to run counter to the following observed facts: a lowering in testosterone levels and an increase in the incidence of undescended testes, in addition to sterility, in males with multiple X chromosomes; abnormalities of the testes in autosomal trisomies; phenotypic abnormalities of XX males apparently increasing with decreasing amounts of Y-chromosomal material; the occurrence of patients with gonadal dysgenesis and XY males with ambiguous genitalia in the same sibship; the occurrence of identical SRY mutations in patients with gonadal dysgenesis and fertile males in the same pedigree; and the development of XY female and hermaphrodite mice having the same genetic constitution.]. 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:1634224; 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:NP205774.RAV9fEktj4dg62OtOJ3q7W-B0QXUJA86tis-1bm5ooyMw130_publicationInfo { this: dcterms:created "2014-10-02T12:33:53+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }