Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_assertion> ?p ?o ?g. }
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- NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_assertion type Assertion NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_head.
- NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_assertion wasGeneratedBy ECO_0000203 NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_provenance.
- NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_assertion wasDerivedFrom befree-20150227 NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_provenance.
- NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_assertion SIO_000772 19239083 NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_provenance.
- NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_assertion evidence source_evidence_literature NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_provenance.
- NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_assertion description "[The ankyloblepharon-ectodermal defects-cleft lip and palate (Hay-Wells or AEC) and the Rapp-Hodgkin syndrome (RHS) are rare autosomal dominant ectodermal dysplasias due to mutations in the transcription factor gene P63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767806.RALfNQoGc4PsDl3v6sFFC0Ubil01TH32OVHctJzIWi7ac130_provenance.