Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_assertion> ?p ?o ?g. }
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- NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_assertion type Assertion NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_head.
- NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_assertion wasGeneratedBy ECO_0000203 NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_provenance.
- NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_assertion wasDerivedFrom befree-2016 NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_provenance.
- NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_assertion SIO_000772 17224651 NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_provenance.
- NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_assertion evidence source_evidence_literature NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_provenance.
- NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_assertion description "[Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, orofacial clefting and limb malformations as the key characteristics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588977.RAPpuQ02dv5W8Oc_OB9OyhnD9dlzdmOyN7xny2AhFdits130_provenance.