@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:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_head { this: np:hasAssertion dgn-np:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_assertion; np:hasProvenance dgn-np:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_provenance; np:hasPublicationInfo dgn-np:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_publicationInfo; a np:Nanopublication . dgn-np:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_assertion a np:Assertion . dgn-np:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_provenance a np:Provenance . dgn-np:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_publicationInfo a np:PublicationInfo . } dgn-np:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_assertion { miriam-gene:9469 a ncit:C16612 . lld:C0342471 a ncit:C7057 . dgn-gda:DGNfc4fc05db0e160132f52ec10b5415253 sio:SIO_000628 miriam-gene:9469, lld:C0342471; a sio:SIO_001121 . } dgn-np:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_provenance { dgn-np:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_assertion dcterms:description "[These findings suggest that the degree of ACTH-stimulated delta 5 precursor steroid abnormality, such as delta 5-17P levels up to 10 SD above the normal mean level found in our PP patients, is not caused by a mild variant of 3 beta HSD deficiency CAH resulting from type II or type I 3 beta HSD gene mutation.]. 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:8923844; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP824371.RAnQ4Z9j8wyahz9-Gf3t9klEhFeM0uW7_d0M5v4-z4qhI130_publicationInfo { this: dcterms:created "2015-08-25T14:45:59+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }