@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:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_head { this: np:hasAssertion dgn-np:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_assertion; np:hasProvenance dgn-np:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_provenance; np:hasPublicationInfo dgn-np:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_publicationInfo; a np:Nanopublication . dgn-np:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_assertion a np:Assertion . dgn-np:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_provenance a np:Provenance . dgn-np:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_publicationInfo a np:PublicationInfo . } dgn-np:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_assertion { miriam-gene:80326 a ncit:C16612 . lld:C1275074 a ncit:C7057 . dgn-gda:DGN0c47fddbff29976186978d9be27045fd sio:SIO_000628 miriam-gene:80326, lld:C1275074; a sio:SIO_001121 . } dgn-np:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_provenance { dgn-np:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_assertion dcterms:description "[In this study, we show that (1) WNT10A mutations cause not only OODD but also other forms of ectodermal dysplasia, reaching from apparently monosymptomatic severe oligodontia to Schöpf-Schulz-Passarge syndrome, which is so far considered a unique entity by the findings of numerous cysts along eyelid margins and the increased risk of benign and malignant skin tumors; (2) WNT10A mutations are a frequent cause of ectodermal dysplasia and were found in about 9% of an unselected patient cohort; (3) about half of the heterozygotes (53.8%) show a phenotype manifestation, including mainly tooth and nail anomalies, which was not reported before in OODD; and (4) heterozygotes show a sex-biased manifestation pattern, with a significantly higher proportion of tooth anomalies in males than in females, which may implicate gender-specific differences of WNT10A expression.]. 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:19559398; 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:NP747810.RAQ9zmf75U6GXvv9PNQ6qrFvLWwMxUHvse94uK4qZqeEY130_publicationInfo { this: dcterms:created "2016-05-13T12:47:24+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }